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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122821copy number variation1nstd186human GRCh37 chr8: 42,920,331-42,921,654 , GRCh38.p12 chr8: 43,065,188-43,066,511 FNTA
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5916433copy number variation1nstd209human GRCh38 chr8: 43,065,499-43,066,510 , GRCh37.p13 chr8: 42,920,642-42,921,653 FNTA
    nsv5915925copy number variation1nstd209human GRCh38 chr8: 42,947,015-43,232,140 , GRCh37.p13 chr8: 42,802,158-43,087,283 FNTA, POMK, 6 more genes
    nsv5861422copy number variation1nstd209human GRCh38 chr8: 43,053,878-43,063,862 , GRCh37.p13 chr8: 42,909,021-42,919,005 FNTA
    nsv5861338copy number variation1nstd209human GRCh38 chr8: 43,080,904-43,084,003 , GRCh37.p13 chr8: 42,936,047-42,939,146 FNTA
    nsv5855935copy number variation2nstd209human GRCh38 chr8: 43,065,178-43,066,917 , GRCh37.p13 chr8: 42,920,321-42,922,060 FNTA
    nsv5850637copy number variation2nstd209human GRCh38 chr8: 43,081,704-43,105,846 , GRCh37.p13 chr8: 42,936,847-42,960,989 FNTA, POMK
    nsv5573757copy number variation1nstd207human GRCh38 chr8: 43,065,499-43,066,510 , GRCh37.p13 chr8: 42,920,642-42,921,653 FNTA
    nsv5475960copy number variation1nstd206human GRCh38 chr8: 43,065,188-43,066,511 , GRCh37.p13 chr8: 42,920,331-42,921,654 FNTA
    nsv5317075copy number variation1nstd204human GRCh38.p13 chr8: 43,065,506-43,066,536 , GRCh37.p13 chr8: 42,920,649-42,921,679 FNTA
    nsv5253096copy number variation1nstd204human GRCh38.p13 chr8: 43,065,478-43,066,541 , GRCh37.p13 chr8: 42,920,621-42,921,684 FNTA
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5113143mobile element insertion1nstd203human GRCh38 chr8: 43,085,855-43,085,871 , GRCh37.p13 chr8: 42,940,998-42,941,014 FNTA
    nsv5108909mobile element insertion1nstd203human GRCh38 chr8: 43,068,072-43,068,072 , GRCh37.p13 chr8: 42,923,215-42,923,215 FNTA
    nsv5108113mobile element insertion1nstd203human GRCh38 chr8: 43,072,759-43,072,767 , GRCh37.p13 chr8: 42,927,902-42,927,910 RNU1-124P, FNTA
    nsv5101661mobile element insertion1nstd203human GRCh38 chr8: 43,063,565-43,063,569 , GRCh37.p13 chr8: 42,918,708-42,918,712 FNTA
    nsv4967189copy number variation1nstd200human GRCh38 chr8: 43,066,536-43,068,124 , GRCh37.p13 chr8: 42,921,679-42,923,267 FNTA
    nsv4967188copy number variation1nstd200human GRCh38 chr8: 43,065,535-43,066,511 , GRCh37.p13 chr8: 42,920,678-42,921,654 FNTA
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