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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906788copy number variation1nstd209human GRCh38 chr2: 226,757,405-226,757,482 , GRCh37.p13 chr2: 227,622,121-227,622,198 IRS1
    nsv5888285copy number variation1nstd209human GRCh38 chr2: 226,780,963-226,781,196 , GRCh37.p13 chr2: 227,645,679-227,645,912 IRS1
    nsv5719768mobile element insertion2nstd211human GRCh38 chr2: 226,757,954-226,757,954 , GRCh37.p13 chr2: 227,622,670-227,622,670 IRS1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5542915insertion1nstd206human GRCh38 chr2: 226,748,349-226,748,387 , GRCh37.p13 chr2: 227,613,065-227,613,103 IRS1
    nsv5451079copy number variation1nstd206human GRCh38 chr2: 226,780,966-226,781,197 , GRCh37.p13 chr2: 227,645,682-227,645,913 IRS1
    nsv5450106copy number variation1nstd206human GRCh38 chr2: 226,776,678-226,782,820 , GRCh37.p13 chr2: 227,641,394-227,647,536 IRS1
    nsv5442704copy number variation1nstd206human GRCh38 chr2: 226,757,407-226,757,483 , GRCh37.p13 chr2: 227,622,123-227,622,199 IRS1
    nsv5201565copy number variation1nstd204human GRCh38.p13 chr2: 226,471,101-227,202,700 , GRCh37.p13 chr2: 227,335,817-228,067,416 COL4A3, MIR5702, 3 more genes
    nsv5161463mobile element insertion1nstd203human GRCh38 chr2: 226,786,676-226,786,676 , GRCh37.p13 chr2: 227,651,392-227,651,392 IRS1
    nsv5061259mobile element insertion1nstd203human GRCh38 chr2: 226,748,336-226,748,349 , GRCh37.p13 chr2: 227,613,052-227,613,065 IRS1
    nsv4914001copy number variation1nstd200human GRCh38 chr2: 226,780,188-226,785,479 , GRCh37.p13 chr2: 227,644,904-227,650,195 IRS1
    nsv4914000copy number variation1nstd200human GRCh38 chr2: 226,776,611-226,782,883 , GRCh37.p13 chr2: 227,641,327-227,647,599 IRS1
    nsv4913997copy number variation1nstd200human GRCh38 chr2: 226,668,353-226,856,940 , GRCh37.p13 chr2: 227,533,069-227,721,656 RHBDD1, IRS1
    nsv4747131copy number variation1nstd199human GRCh37 chr2: 227,610,960-227,611,105 , GRCh38.p12 chr2: 226,746,244-226,746,389 IRS1
    nsv4728759copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 226,027,074-229,110,812 , GRCh38.p12 chr2: 225,162,357-228,246,096 COL4A3, COL4A4, 28 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4550119insertion1nstd166human GRCh37.p13 chr2: 227,621,515-227,621,515 , GRCh38.p12 chr2: 226,756,799-226,756,799 IRS1
    nsv4549947insertion1nstd166human GRCh37.p13 chr2: 227,613,052-227,613,052 , GRCh38.p12 chr2: 226,748,336-226,748,336 IRS1
    nsv4519259copy number variation1nstd166human GRCh37.p13 chr2: 227,622,123-227,622,199 , GRCh38.p12 chr2: 226,757,407-226,757,483 IRS1
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