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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917003copy number variation1nstd229human GRCh38 chr11: 55,841,272-55,845,254 , GRCh37.p13 chr11: 55,608,748-55,612,730 OR5D16
    nsv6621250copy number variation1nstd224human GRCh37 chr11: 55,595,455-55,690,371 , GRCh38.p12 chr11: 55,827,979-55,922,895 OR5L2, OR9M1P, 6 more genes
    nsv6621249copy number variation1nstd224human GRCh37 chr11: 55,171,027-56,905,911 , GRCh38.p12 chr11: 55,403,551-57,138,437 OR5I1, OR8K2P, 113 more genes
    nsv6621186copy number variation2nstd224human GRCh37 chr11: 54,794,237-56,003,589 , GRCh38.p12 chr11: 55,026,761-56,236,113 OR5L2, OR9M1P, 65 more genes
    nsv6621001copy number variation2nstd224human GRCh37 chr11: 55,594,936-55,690,371 , GRCh38.p12 chr11: 55,827,460-55,922,895 OR5L2, OR9M1P, 6 more genes
    nsv6620768copy number variation1nstd224human GRCh37 chr11: 55,068,237-55,605,002 , GRCh38.p12 chr11: 55,300,761-55,837,526 OR5D2P, OR4C1P, 31 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6131996copy number variation1nstd213human GRCh37 chr11: 55,349,448-55,758,508 , GRCh38.p12 chr11: 55,581,972-55,991,032 OR5D3P, OR5D2P, 25 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5923433copy number variation1nstd209human GRCh38 chr11: 55,842,983-55,843,080 , GRCh37.p13 chr11: 55,610,459-55,610,556 OR5D16
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5913053copy number variation1nstd209human GRCh38 chr11: 55,268,110-55,880,081 , GRCh37.p13 chr11: 55,035,586-55,647,557 OR4A50P, OR9M1P, 36 more genes
    nsv5909729copy number variation1nstd209human GRCh38 chr11: 55,500,571-56,102,471 , GRCh37.p13 chr11: 55,268,047-55,869,947 OR10AG1, OR5D17P, 37 more genes
    nsv5561297sequence alteration1nstd206human GRCh38 chr11: 55,833,210-55,838,438 , GRCh37.p13 chr11: 55,600,686-55,605,914 OR5D16
    nsv5511252copy number variation1nstd206human GRCh38 chr11: 55,833,129-55,838,438 , GRCh37.p13 chr11: 55,600,605-55,605,914 OR5D16
    nsv5504810copy number variation1nstd206human GRCh38 chr11: 55,842,986-55,843,081 , GRCh37.p13 chr11: 55,610,462-55,610,557 OR5D16
    nsv5500828copy number variation1nstd206human GRCh38 chr11: 55,825,364-55,927,988 , GRCh37.p13 chr11: 55,592,840-55,695,464 OR5L2, OR9M1P, 6 more genes
    nsv5500007copy number variation1nstd206human GRCh38 chr11: 55,843,290-55,843,781 , GRCh37.p13 chr11: 55,610,766-55,611,257 OR5D16
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
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