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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949321insertion1nstd209human GRCh38 chr7: 55,791,615-55,791,615 , GRCh37.p13 chr7: 55,859,308-55,859,308 SEPTIN14
    nsv5927524copy number variation1nstd209human GRCh38 chr7: 55,836,992-55,837,137 , GRCh37.p13 chr7: 55,904,685-55,904,830 SEPTIN14
    nsv5920391copy number variation1nstd209human GRCh38 chr7: 55,822,496-55,822,572 , GRCh37.p13 chr7: 55,890,189-55,890,265 SEPTIN14
    nsv5919608copy number variation1nstd209human GRCh38 chr7: 55,829,690-55,829,778 , GRCh37.p13 chr7: 55,897,383-55,897,471 SEPTIN14
    nsv5917709copy number variation1nstd209human GRCh38 chr7: 55,854,677-55,855,256 , GRCh37.p13 chr7: 55,922,370-55,922,949 SEPTIN14
    nsv5914455copy number variation1nstd209human GRCh38 chr7: 55,796,325-55,806,057 , GRCh37.p13 chr7: 55,864,018-55,873,750 CICP12, SEPTIN14
    nsv5913807copy number variation1nstd209human GRCh38 chr7: 55,813,547-55,813,640 , GRCh37.p13 chr7: 55,881,240-55,881,333 SEPTIN14
    nsv5912235copy number variation1nstd209human GRCh38 chr7: 55,836,645-55,841,941 , GRCh37.p13 chr7: 55,904,338-55,909,634 SEPTIN14
    nsv5847333copy number variation1nstd209human GRCh38 chr7: 55,796,353-55,805,738 , GRCh37.p13 chr7: 55,864,046-55,873,431 CICP12, SEPTIN14
    nsv5846750copy number variation2nstd209human GRCh38 chr7: 55,803,114-55,805,813 , GRCh37.p13 chr7: 55,870,807-55,873,506 SEPTIN14
    nsv5729925mobile element insertion1nstd211human GRCh38 chr7: 55,828,004-55,828,004 , GRCh37.p13 chr7: 55,895,697-55,895,697 SEPTIN14
    nsv5685705mobile element insertion2nstd211human GRCh38 chr7: 55,846,092-55,846,092 , GRCh37.p13 chr7: 55,913,785-55,913,785 SEPTIN14
    nsv5680087mobile element insertion2nstd211human GRCh38 chr7: 55,847,865-55,847,865 , GRCh37.p13 chr7: 55,915,558-55,915,558 SEPTIN14
    nsv5641606insertion1nstd207human GRCh38 chr7: 55,813,547-55,813,547 , GRCh37.p13 chr7: 55,881,240-55,881,240 SEPTIN14
    nsv5637995insertion1nstd207human GRCh38 chr7: 55,855,008-55,855,008 , GRCh37.p13 chr7: 55,922,701-55,922,701 SEPTIN14
    nsv5628247insertion1nstd207human GRCh38 chr7: 55,854,677-55,854,677 , GRCh37.p13 chr7: 55,922,370-55,922,370 SEPTIN14
    nsv5561957sequence alteration1nstd206human GRCh38 chr7: 55,828,459-55,830,654 , GRCh37.p13 chr7: 55,896,152-55,898,347 SEPTIN14
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5550892insertion1nstd206human GRCh38 chr7: 55,847,865-55,847,900 , GRCh37.p13 chr7: 55,915,558-55,915,593 SEPTIN14
    nsv5543476insertion1nstd206human GRCh38 chr7: 55,826,057-55,826,057 , GRCh37.p13 chr7: 55,893,750-55,893,750 SEPTIN14
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