{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:4851","source":"HGNC:4851|huntingtin","targets":["1393012|NM_001388492.1(HTT):c.2710C>T (p.Gln904Ter)|single nucleotide variant|Pathogenic|HTT|criteria provided, single submitter|4","1464611|NM_001388492.1(HTT):c.2085del (p.Gly697fs)|Deletion|Pathogenic|HTT|criteria provided, single submitter|4","1494729|NM_001388492.1(HTT):c.5821_5833del (p.Ser1941fs)|Deletion|Pathogenic|HTT|criteria provided, single submitter|4","1808621|GRCh37/hg19 4p16.3-15.33(chr4:1-12785001)x1|copy number loss|Pathogenic|HTT|criteria provided, single submitter|4","409|NC_000004.11:g.3076606GCA[40_?]|Microsatellite|Pathogenic|HTT|practice guideline|4","417745|NM_001388492.1(HTT):c.8150T>A (p.Phe2717Tyr)|single nucleotide variant|Pathogenic|HTT|no assertion criteria provided|4"]}]}