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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973985insertion1nstd209human GRCh38 chr12: 9,258,218-9,258,218 , GRCh37.p13 chr12: 9,410,814-9,410,814 LINC00987
    nsv5861701copy number variation1nstd209human GRCh38 chr12: 9,238,025-9,241,371 , GRCh37.p13 chr12: 9,390,621-9,393,967 MIR1244-3, LINC00987, 1 more genes
    nsv5710214mobile element insertion1nstd211human GRCh38 chr12: 9,261,582-9,261,582 , GRCh37.p13 chr12: 9,414,178-9,414,178 LINC00987
    nsv5655076insertion1nstd207human GRCh38 chr12: 9,258,218-9,258,218 , GRCh37.p13 chr12: 9,410,814-9,410,814 LINC00987
    nsv5548890insertion1nstd206human GRCh38 chr12: 9,258,219-9,258,219 , GRCh37.p13 chr12: 9,410,815-9,410,815 LINC00987
    nsv5426960mobile element insertion1nstd206human GRCh38 chr12: 9,261,582-9,261,633 , GRCh37.p13 chr12: 9,414,178-9,414,229 LINC00987
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5262888copy number variation1nstd204human GRCh38.p13 chr12: 9,239,701-9,240,200 , GRCh37.p13 chr12: 9,392,297-9,392,796 LINC00987, PTMAP4, 1 more genes
    nsv5130699mobile element insertion1nstd203human GRCh38 chr12: 9,253,000-9,253,016 , GRCh37.p13 chr12: 9,405,596-9,405,612 LINC00987
    nsv5126716mobile element insertion1nstd203human GRCh38 chr12: 9,244,375-9,244,391 , GRCh37.p13 chr12: 9,396,971-9,396,987 LINC00987
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4764940insertion1nstd199human GRCh37 chr12: 9,410,812-9,410,812 , GRCh38.p12 chr12: 9,258,216-9,258,216 LINC00987
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4616968copy number variation1nstd183human GRCh37 chr12: 9,368,676-9,456,821 , GRCh38.p12 chr12: 9,216,080-9,304,225 A2MP1, PTMAP4, 4 more genes
    nsv4616824copy number variation1nstd183human GRCh37 chr12: 8,488,721-9,625,223 , GRCh38.p12 chr12: 8,336,125-9,472,627 , BTG1P1, 43 more genes
    nsv4609577copy number variation1nstd183human GRCh37 chr12: 9,305,636-9,546,438 , GRCh38.p12 chr12: 9,153,040-9,393,842 , A2MP1, 10 more genes
    nsv4553384insertion1nstd166human GRCh37.p13 chr12: 9,395,806-9,395,806 , GRCh38.p12 chr12: 9,243,210-9,243,210 LINC00987
    nsv4508937mobile element insertion1nstd166human GRCh37.p13 chr12: 9,405,596-9,405,596 , GRCh38.p12 chr12: 9,253,000-9,253,000 LINC00987
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
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