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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6916316copy number variation1nstd229human GRCh38 chr11: 4,495,101-4,614,600 , GRCh37.p13 chr11: 4,516,331-4,635,830 OR52M2P, OR52I2, 4 more genes
    nsv6916237copy number variation1nstd229human GRCh38 chr11: 4,369,424-4,697,710 , GRCh37.p13 chr11: 4,390,654-4,718,940 TRIM68, OR51E2, 17 more genes
    nsv6916129copy number variation1nstd229human GRCh38 chr11: 3,833,721-4,728,036 , GRCh37.p13 chr11: 3,854,951-4,749,266 OR52K1, OR52B4, 39 more genes
    nsv6914951copy number variation1nstd229human GRCh38 chr11: 4,515,180-4,719,642 , GRCh37.p13 chr11: 4,536,410-4,740,872 OR51A9P, OR52M1, 12 more genes
    nsv6910853copy number variation1nstd229human GRCh38 chr11: 4,496,473-4,621,051 , GRCh37.p13 chr11: 4,517,703-4,642,281 C11orf40, OR52I1, 4 more genes
    nsv6907396copy number variation1nstd229human GRCh38 chr11: 4,560,919-4,669,992 , GRCh37.p13 chr11: 4,582,149-4,691,222 TRIM68, OR52I2, 6 more genes
    nsv6900520copy number variation1nstd229human GRCh38 chr11: 4,562,140-4,616,444 , GRCh37.p13 chr11: 4,583,370-4,637,674 TRIM68, C11orf40, 2 more genes
    nsv6638006copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,384,773-4,681,230 , GRCh38.p12 chr11: 4,363,543-4,660,000 OR51R1P, OR52I1, 15 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6445528copy number variation1nstd223human GRCh38 chr11: 4,495,092-4,614,586 , GRCh37.p13 chr11: 4,516,322-4,635,816 TRIM68, OR52M1, 4 more genes
    nsv6442818copy number variation1nstd223human GRCh38 chr11: 4,560,601-4,670,000 , GRCh37.p13 chr11: 4,581,831-4,691,230 TRIM68, C11orf40, 6 more genes
    nsv6438415copy number variation1nstd223human GRCh38 chr11: 4,449,872-4,656,651 , GRCh37.p13 chr11: 4,471,102-4,677,881 OR52I1, OR52K2, 9 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6132106copy number variation1nstd213human GRCh37 chr11: 4,510,000-5,300,001 , GRCh38.p12 chr11: 4,488,770-5,278,771 HBB, HBBP1, 57 more genes
    nsv5857592copy number variation2nstd209human GRCh38 chr11: 4,587,191-4,592,931 , GRCh37.p13 chr11: 4,608,421-4,614,161 OR52I1, OR52I2
    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
    nsv5508306copy number variation1nstd206human GRCh38 chr11: 4,586,000-4,594,200 , GRCh37.p13 chr11: 4,607,230-4,615,430 OR52I2, OR52I1
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