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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5856580copy number variation2nstd209human GRCh38 chr11: 4,587,588-4,597,558 , GRCh37.p13 chr11: 4,608,818-4,618,788 TRIM68, OR52I2, 1 more genes
    nsv5257404copy number variation1nstd204human GRCh38.p13 chr11: 4,589,732-4,622,516 , GRCh37.p13 chr11: 4,610,962-4,643,746 OR52I1, TRIM68
    nsv5251636copy number variation1nstd204human GRCh38.p13 chr11: 4,524,901-4,620,000 , GRCh37.p13 chr11: 4,546,131-4,641,230 OR52I2, OR52M1, 3 more genes
    nsv4977964copy number variation1nstd200human GRCh38 chr11: 4,560,919-4,669,991 , GRCh37.p13 chr11: 4,582,149-4,691,221 TRIM68, C11orf40, 6 more genes
    nsv4977955copy number variation1nstd200human GRCh38 chr11: 4,495,092-4,614,586 , GRCh37.p13 chr11: 4,516,322-4,635,816 TRIM68, OR52M1, 4 more genes
    nsv4977953copy number variation1nstd200human GRCh38 chr11: 4,449,871-4,656,651 , GRCh37.p13 chr11: 4,471,101-4,677,881 OR52M1, OR52K1, 9 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4728922copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,388,904-4,639,840 , GRCh38.p12 chr11: 4,367,674-4,618,610 OR52K1, OR52B4, 12 more genes
    nsv4679088copy number variation1nstd189human GRCh37.p13 chr11: 4,335,879-4,833,224 , GRCh38.p12 chr11: 4,314,649-4,811,994 TRIM21, TRIM68, 29 more genes
    nsv4678966copy number variation1nstd189human GRCh37.p13 chr11: 4,578,465-4,689,637 , GRCh38.p12 chr11: 4,557,235-4,668,407 TRIM68, C11orf40, 6 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4606954copy number variation1nstd183human GRCh37 chr11: 4,586,670-4,686,839 , GRCh38.p12 chr11: 4,565,440-4,665,609 TRIM68, C11orf40, 6 more genes
    nsv4599432copy number variation1nstd183human GRCh37 chr11: 4,582,150-4,687,238 , GRCh38.p12 chr11: 4,560,920-4,666,008 TRIM68, C11orf40, 6 more genes
    nsv4414636copy number variation1nstd174human GRCh37 chr11: 4,582,150-4,687,238 , GRCh38.p12 chr11: 4,560,920-4,666,008 TRIM68, C11orf40, 6 more genes
    nsv4413914copy number variation1nstd174human GRCh37 chr11: 4,519,222-4,630,740 , GRCh38.p12 chr11: 4,497,992-4,609,510 TRIM68, OR52M1, 4 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 more genes
    nsv4377870copy number variation1nstd173human GRCh37 chr11: 4,515,398-4,636,371 , GRCh38.p12 chr11: 4,494,168-4,615,141 TRIM68, OR52M1, 4 more genes
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