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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128902copy number variation1nstd186human GRCh37 chr22: 46,690,159-46,690,492 , GRCh38.p12 chr22: 46,294,262-46,294,595 GTSE1, TTC38, 1 more genes
    nsv5966810copy number variation1nstd209human GRCh38 chr22: 46,305,338-46,305,636 , GRCh37.p13 chr22: 46,701,235-46,701,533 GTSE1
    nsv5952614copy number variation1nstd209human GRCh38 chr22: 46,294,262-46,294,593 , GRCh37.p13 chr22: 46,690,159-46,690,490 GTSE1, TTC38, 1 more genes
    nsv5949386copy number variation1nstd209human GRCh38 chr22: 46,306,217-46,306,515 , GRCh37.p13 chr22: 46,702,114-46,702,412 GTSE1
    nsv5601984copy number variation1nstd207human GRCh38 chr22: 46,294,251-46,294,582 , GRCh37.p13 chr22: 46,690,148-46,690,479 GTSE1, TTC38, 1 more genes
    nsv5541587copy number variation1nstd206human GRCh38 chr22: 46,323,745-46,345,185 , GRCh37.p13 chr22: 46,719,642-46,741,082 GTSE1, TRMU
    nsv5537636copy number variation1nstd206human GRCh38 chr22: 46,294,262-46,294,595 , GRCh37.p13 chr22: 46,690,159-46,690,492 GTSE1, GTSE1-DT, 1 more genes
    nsv5533994copy number variation1nstd206human GRCh38 chr22: 46,312,410-46,312,933 , GRCh37.p13 chr22: 46,708,307-46,708,830 GTSE1
    nsv5391579copy number variation1nstd186human GRCh37 chr22: 46,690,219-46,690,492 , GRCh38.p12 chr22: 46,294,322-46,294,595 GTSE1, TTC38, 1 more genes
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5282808copy number variation1nstd204human GRCh38.p13 chr22: 46,294,301-46,294,600 , GRCh37.p13 chr22: 46,690,198-46,690,497 GTSE1-DT, GTSE1, 1 more genes
    nsv5032814copy number variation1nstd200human GRCh38 chr22: 46,266,177-46,420,843 , GRCh37.p13 chr22: 46,662,074-46,816,740 TRMU, TTC38, 3 more genes
    nsv4886474copy number variation1nstd200human GRCh37 chr22: 46,690,217-46,690,493 , GRCh38.p12 chr22: 46,294,320-46,294,596 TTC38, GTSE1-DT, 1 more genes
    nsv4873835copy number variation1nstd200human GRCh37 chr22: 46,708,351-46,708,808 , GRCh38.p12 chr22: 46,312,454-46,312,911 GTSE1
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4703910copy number variation1nstd195human GRCh38.p12 chr22: 46,294,251-46,294,252 , GRCh37 chr22: 46,690,148-46,690,149 GTSE1, TTC38, 1 more genes
    nsv4685973copy number variation1nstd102humanPathogenic GRCh38 chr22: 45,708,330-50,737,364 , GRCh37.p13 chr22: 46,104,210-51,175,792 PRR34, KLHDC7B, 102 more genes
    nsv4685945copy number variation1nstd102humanPathogenic GRCh38 chr22: 43,032,129-50,739,836 , GRCh37.p13 chr22: 43,428,135-51,178,264 LOC101927474, SHISAL1, 165 more genes
    nsv4685937copy number variation1nstd102humanPathogenic GRCh38 chr22: 43,802,117-50,806,121 , GRCh37.p13 chr22: 44,197,997-51,203,353 CIMAP1B, PNPLA3, 151 more genes
    nsv4685915copy number variation1nstd102humanPathogenic GRCh38 chr22: 44,702,479-50,806,138 , GRCh37.p13 chr22: 45,098,359-51,203,353 LOC105373066, LOC339685, 130 more genes
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