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Items: 1 to 20 of 359

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130889insertion1nstd186human GRCh37 chr19: 22,819,724-22,819,724 , GRCh38.p12 chr19: 22,636,922-22,636,922 ZNF492
    nsv6114065mobile element insertion1nstd186human GRCh37 chr19: 22,816,842-22,816,878 , GRCh38.p12 chr19: 22,634,040-22,634,076 ZNF492
    nsv5974152inversion1nstd209human GRCh38 chr19: 22,346,882-22,718,617 , GRCh37.p13 chr19: 22,529,684-22,901,419 ZNF492, ZNF98, 17 more genes
    nsv5971394insertion1nstd209human GRCh38 chr19: 22,634,027-22,634,027 , GRCh37.p13 chr19: 22,816,829-22,816,829 ZNF492
    nsv5970763insertion1nstd209human GRCh38 chr19: 22,636,886-22,636,886 , GRCh37.p13 chr19: 22,819,688-22,819,688 ZNF492
    nsv5947141copy number variation1nstd209human GRCh38 chr19: 22,655,917-22,659,757 , GRCh37.p13 chr19: 22,838,719-22,842,559 ZNF492
    nsv5940544copy number variation1nstd209human GRCh38 chr19: 21,933,481-22,933,189 , GRCh37.p13 chr19: 22,116,283-23,115,991 , BNIP3P33, 42 more genes
    nsv5940238copy number variation1nstd209human GRCh38 chr19: 22,665,066-22,665,149 , GRCh37.p13 chr19: 22,847,868-22,847,951 ZNF492
    nsv5939524copy number variation1nstd209human GRCh38 chr19: 21,932,270-22,932,025 , GRCh37.p13 chr19: 22,115,072-23,114,827 , ZNF676, 42 more genes
    nsv5868363copy number variation1nstd209human GRCh38 chr19: 22,655,874-22,658,239 , GRCh37.p13 chr19: 22,838,676-22,841,041 ZNF492
    nsv5705163mobile element insertion1nstd211human GRCh38 chr19: 22,653,544-22,653,544 , GRCh37.p13 chr19: 22,836,346-22,836,346 ZNF492
    nsv5698653mobile element insertion2nstd211human GRCh38 chr19: 22,655,694-22,655,694 , GRCh37.p13 chr19: 22,838,496-22,838,496 ZNF492
    nsv5697329mobile element insertion1nstd211human GRCh38 chr19: 22,634,040-22,634,040 , GRCh37.p13 chr19: 22,816,842-22,816,842 ZNF492
    nsv5649768insertion1nstd207human GRCh38 chr19: 22,634,027-22,634,027 , GRCh37.p13 chr19: 22,816,829-22,816,829 ZNF492
    nsv5647925insertion1nstd207human GRCh38 chr19: 22,636,886-22,636,886 , GRCh37.p13 chr19: 22,819,688-22,819,688 ZNF492
    nsv5597466copy number variation1nstd207human GRCh38 chr19: 22,652,221-22,652,387 , GRCh37.p13 chr19: 22,835,023-22,835,189 ZNF492
    nsv5559833sequence alteration1nstd206human GRCh38 chr19: 22,337,409-22,727,937 , GRCh37.p13 chr19: 22,520,211-22,910,739 LINC01785, ZNF849P, 17 more genes
    nsv5544824insertion1nstd206human GRCh38 chr19: 22,636,922-22,636,922 , GRCh37.p13 chr19: 22,819,724-22,819,724 ZNF492
    nsv5531583copy number variation1nstd206human GRCh38 chr19: 22,650,389-22,654,363 , GRCh37.p13 chr19: 22,833,191-22,837,165 ZNF492
    nsv5526651copy number variation1nstd206human GRCh38 chr19: 21,859,999-22,962,000 , GRCh37.p13 chr19: 22,042,801-23,144,802 , RAD54L2P1, 45 more genes
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