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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5951896copy number variation1nstd209human GRCh38 chr20: 62,294,456-62,295,273 , GRCh37.p13 chr20: 60,869,512-60,870,329 OSBPL2
    nsv5672207insertion1nstd207human GRCh38 chr20: 62,291,826-62,291,826 , GRCh37.p13 chr20: 60,866,882-60,866,882 OSBPL2
    nsv5669063insertion1nstd207human GRCh38 chr20: 62,278,566-62,278,566 , GRCh37.p13 chr20: 60,853,622-60,853,622 OSBPL2
    nsv5598488copy number variation1nstd207human GRCh38 chr20: 62,270,578-62,270,707 , GRCh37.p13 chr20: 60,845,634-60,845,763 OSBPL2
    nsv5592061copy number variation1nstd207human GRCh38 chr20: 62,278,549-62,278,687 , GRCh37.p13 chr20: 60,853,605-60,853,743 OSBPL2
    nsv5589776copy number variation1nstd207human GRCh38 chr20: 62,270,414-62,270,468 , GRCh37.p13 chr20: 60,845,470-60,845,524 OSBPL2
    nsv5585090copy number variation1nstd207human GRCh38 chr20: 62,270,676-62,270,739 , GRCh37.p13 chr20: 60,845,732-60,845,795 OSBPL2
    nsv5526248copy number variation1nstd206human GRCh38 chr20: 62,249,692-62,251,526 , GRCh37.p13 chr20: 60,824,748-60,826,582 OSBPL2
    nsv5519320copy number variation1nstd206human GRCh38 chr20: 62,294,459-62,295,274 , GRCh37.p13 chr20: 60,869,515-60,870,330 OSBPL2
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5350547translocation1nstd200human GRCh38 chr20: 62,295,274-62,295,274 , GRCh38 chr20: 62,294,459-62,294,459 , GRCh37.p13 chr20: 60,870,330-60,870,330 , GRCh37.p13 chr20: 60,869,515-60,869,515 OSBPL2
    nsv5326110copy number variation1nstd204human GRCh38.p13 chr20: 62,294,449-62,295,283 , GRCh37.p13 chr20: 60,869,505-60,870,339 OSBPL2
    nsv5289201copy number variation1nstd204human GRCh38.p13 chr20: 62,058,601-62,909,300 , GRCh37.p13 chr20: 60,633,657-61,540,652 , LOC105372716, 47 more genes
    nsv5284819copy number variation1nstd204human GRCh38.p13 chr20: 62,134,401-62,423,600 , GRCh37.p13 chr20: 60,709,457-60,998,656 , RPS21, 15 more genes
    nsv5216290mobile element deletion1nstd204human GRCh38.p13 chr20: 62,255,093-62,255,421 , GRCh37.p13 chr20: 60,830,149-60,830,477 OSBPL2
    nsv5173192mobile element insertion1nstd203human GRCh38 chr20: 62,276,930-62,276,943 , GRCh37.p13 chr20: 60,851,986-60,851,999 OSBPL2
    nsv5172096mobile element insertion1nstd203human GRCh38 chr20: 62,267,968-62,268,011 , GRCh37.p13 chr20: 60,843,024-60,843,067 OSBPL2
    nsv5170173mobile element insertion1nstd203human GRCh38 chr20: 62,251,865-62,251,896 , GRCh37.p13 chr20: 60,826,921-60,826,952 OSBPL2
    nsv5167724mobile element insertion1nstd203human GRCh38 chr20: 62,259,920-62,259,930 , GRCh37.p13 chr20: 60,834,976-60,834,986 OSBPL2
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