{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:4827,10,HGNC:4827,102,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:4827","source":"HGNC:4827|hemoglobin subunit beta","targets":["1048666|NC_000011.10:g.5224303_5227790del|Deletion|Pathogenic|HBB|no assertion criteria provided|11","1050837|NM_000518.4(HBB):c.-134A>G|single nucleotide variant|Uncertain significance|HBB|criteria provided, single submitter|11","1065151|NM_000518.5(HBB):c.233_234del (p.His78fs)|Deletion|Likely pathogenic|HBB|criteria provided, multiple submitters, no conflicts|11","1074556|NC_000011.9:g.(?_5247393)_5248785del|Deletion|Pathogenic|HBB|criteria provided, single submitter|","1074558|NC_000011.9:g.(?_5247493)_5248852del|Deletion|Pathogenic|HBB|criteria provided, single submitter|","1074559|NC_000011.9:g.(?_5239576)_5247294del|Deletion|Pathogenic|HBB|criteria provided, single submitter|","1074561|NC_000011.9:g.(?_5246696)_5247105del|Deletion|Pathogenic|HBB|criteria provided, single submitter|","1076533|NC_000011.10:g.5226755_5227283del|Deletion|Pathogenic|HBB|criteria provided, single submitter|11","1077226|NM_000518.5(HBB):c.316-405T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1077470|NM_000518.5(HBB):c.93-17T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1077721|NM_000518.5(HBB):c.315+139G>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1079811|NM_000518.5(HBB):c.315+283G>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1080073|NM_000518.5(HBB):c.315+73A>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1080158|NM_000518.5(HBB):c.315+213T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1081010|NM_000518.5(HBB):c.315+306A>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1081408|NM_000518.5(HBB):c.315+395T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1082749|NM_000518.5(HBB):c.315+143G>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1083541|NM_000518.5(HBB):c.60C>T (p.Asn20=)|single nucleotide variant|Conflicting classifications of pathogenicity|HBB|criteria provided, conflicting classifications|11","1083998|NM_000518.5(HBB):c.316-219_316-218del|Deletion|Likely benign|HBB|criteria provided, single submitter|11","1084243|NM_000518.5(HBB):c.315+277C>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1084273|NM_000518.5(HBB):c.316-405T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1084304|NM_000518.5(HBB):c.315+246C>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1084750|NM_000518.5(HBB):c.315+269_315+270del|Deletion|Likely benign|HBB|criteria provided, single submitter|11","1084859|NM_000518.5(HBB):c.315+292A>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1087637|NM_000518.5(HBB):c.316-159A>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1088500|NM_000518.5(HBB):c.315+349T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1088912|NM_000518.5(HBB):c.315+234T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1089337|NM_000518.5(HBB):c.315+116T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1089483|NM_000518.5(HBB):c.315+211T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1089508|NM_000518.5(HBB):c.316-31C>T|single nucleotide variant|Likely benign|HBB|criteria provided, multiple submitters, no conflicts|11","1089575|NM_000518.5(HBB):c.316-356T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1089678|NM_000518.5(HBB):c.316-104A>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1090479|NM_000518.5(HBB):c.316-370G>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1090534|NM_000518.5(HBB):c.315+331A>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1090577|NM_000518.5(HBB):c.96G>T (p.Leu32=)|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1090894|NM_000518.5(HBB):c.316-315del|Deletion|Likely benign|HBB|criteria provided, single submitter|11","1091288|NM_000518.5(HBB):c.316-244T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1091467|NM_000518.5(HBB):c.316-42del|Deletion|Likely benign|HBB|criteria provided, multiple submitters, no conflicts|11","1092862|NM_000518.5(HBB):c.316-337T>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1092961|NM_000518.5(HBB):c.315+127T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1093303|NM_000518.5(HBB):c.92+15T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1094229|NM_000518.5(HBB):c.315+184T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1094558|NM_000518.5(HBB):c.316-389C>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1094586|NM_000518.5(HBB):c.315+387T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1094628|NM_000518.5(HBB):c.315+258G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1095187|NM_000518.5(HBB):c.316-400T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1095205|NM_000518.5(HBB):c.316-265A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1095434|NM_000518.5(HBB):c.316-261A>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1095859|NM_000518.5(HBB):c.252C>A (p.Gly84=)|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1095878|NM_000518.5(HBB):c.316-129T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1096096|NM_000518.5(HBB):c.92+28T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1096696|NM_000518.5(HBB):c.315+310T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1096888|NM_000518.5(HBB):c.315+48G>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1097054|NM_000518.5(HBB):c.315+213del|Deletion|Likely benign|HBB|criteria provided, single submitter|11","1097250|NM_000518.5(HBB):c.315+306_315+308del|Deletion|Likely benign|HBB|criteria provided, single submitter|11","1098525|NM_000518.5(HBB):c.384G>C (p.Gln128His)|single nucleotide variant|Uncertain significance|HBB|criteria provided, multiple submitters, no conflicts|11","1098798|NM_000518.5(HBB):c.126dup (p.Phe43fs)|Duplication|Likely pathogenic|HBB|criteria provided, single submitter|11","1099709|NM_000518.5(HBB):c.315+212T>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1099874|NM_000518.5(HBB):c.316-67G>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1099906|NM_000518.5(HBB):c.315+58T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1100138|NM_000518.5(HBB):c.315+55T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1100205|NM_000518.5(HBB):c.316-387C>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1101246|NM_000518.5(HBB):c.316-15A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1101564|NM_000518.5(HBB):c.315+232T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1101596|NM_000518.5(HBB):c.315+149G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1101748|NM_000518.5(HBB):c.315+391_315+395del|Deletion|Likely benign|HBB|criteria provided, single submitter|11","1102136|NM_000518.5(HBB):c.315+169A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1104204|NM_000518.5(HBB):c.435G>A (p.Lys145=)|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1104307|NM_000518.5(HBB):c.316-336del|Deletion|Conflicting classifications of pathogenicity|HBB|criteria provided, conflicting classifications|11","1104842|NM_000518.5(HBB):c.316-418G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1105735|NM_000518.5(HBB):c.316-383T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1106731|NM_000518.5(HBB):c.92+40T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1107574|NM_000518.5(HBB):c.315+354G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1108115|NM_000518.5(HBB):c.92+48G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1108644|NM_000518.5(HBB):c.315+317A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1110042|NM_000518.5(HBB):c.315+285T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1110073|NM_000518.5(HBB):c.315+28C>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1110299|NM_000518.5(HBB):c.315+300A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1110755|NM_000518.5(HBB):c.315+265A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1110772|NM_000518.5(HBB):c.315+317A>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1111047|NM_000518.5(HBB):c.315+100G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1111255|NM_000518.5(HBB):c.156T>C (p.Pro52=)|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1111267|NM_000518.5(HBB):c.315+81C>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1111710|NM_000518.5(HBB):c.225C>G (p.Gly75=)|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1111743|NM_000518.5(HBB):c.315+77G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1111753|NM_000518.5(HBB):c.315+394T>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1112903|NM_000518.5(HBB):c.315+391C>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1112986|NM_000518.5(HBB):c.316-229A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1113861|NM_000518.5(HBB):c.315+140A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1114525|NM_000518.5(HBB):c.315+69G>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1114903|NM_000518.5(HBB):c.315+143G>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1115039|NM_000518.5(HBB):c.315+335C>T|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1115280|NM_000518.5(HBB):c.316-99T>G|single nucleotide variant|Likely benign|HBB|criteria provided, multiple submitters, no conflicts|11","1115568|NM_000518.5(HBB):c.315+254T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1116346|NM_000518.5(HBB):c.316-362T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1117654|NM_000518.5(HBB):c.316-386A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1118139|NM_000518.5(HBB):c.316-397T>A|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1118308|NM_000518.5(HBB):c.279C>T (p.His93=)|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1118833|NM_000518.5(HBB):c.92+41A>G|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11","1118834|NM_000518.5(HBB):c.92+26T>C|single nucleotide variant|Likely benign|HBB|criteria provided, single submitter|11"]}]}