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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6621248copy number variation2nstd224human GRCh37 chr11: 55,134,153-55,256,498 , GRCh38.p12 chr11: 55,366,677-55,489,022 OR4A15, OR4A14P, 6 more genes
    nsv6621188copy number variation1nstd224human GRCh37 chr11: 55,110,277-55,171,027 , GRCh38.p12 chr11: 55,342,801-55,403,551 OR4A15, OR4A9P, 1 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
    nsv6621185copy number variation1nstd224human GRCh37 chr11: 54,794,237-55,168,863 , GRCh38.p12 chr11: 55,026,761-55,401,387 TRIM48, OR4A16, 6 more genes
    nsv6621112copy number variation1nstd224human GRCh37 chr11: 54,974,693-55,541,620 , GRCh38.p12 chr11: 55,207,217-55,774,144 OR5D17P, OR4A15, 27 more genes
    nsv6621000copy number variation1nstd224human GRCh37 chr11: 55,134,153-55,303,865 , GRCh38.p12 chr11: 55,366,677-55,536,389 OR4A21P, OR4A15, 9 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
    nsv6620766copy number variation1nstd224human GRCh37 chr11: 54,847,856-55,193,753 , GRCh38.p12 chr11: 55,080,380-55,426,277 TRIM48, OR4A16, 7 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
    nsv6248083mobile element insertion1nstd215human GRCh38 chr11: 55,369,196-55,369,196 , GRCh37.p13 chr11: 55,136,672-55,136,672 OR4A15
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv6029254copy number variation1nstd212human GRCh37.p13 chr11: 55,121,077-55,252,196 , GRCh38 chr11: 55,353,601-55,484,720 OR4A15, OR4A14P, 6 more genes
    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
    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
    nsv5331756translocation1nstd200human GRCh37 chr11: 55,133,834-55,133,834 , GRCh37 chr11: 55,133,755-55,133,755 , GRCh38.p12 chr11: 55,366,279-55,366,279 , GRCh38.p12 chr11: 55,366,358-55,366,358 OR4A15
    nsv5314140copy number variation1nstd204human GRCh38.p13 chr11: 54,936,175-56,244,178 , GRCh37.p13 chr11: 54,711,405-56,011,654 OR5D18, OR5BE1P, 65 more genes
    nsv5308204copy number variation1nstd204human GRCh37.p13 chr11: 55,091,831-55,188,738 , GRCh38.p13 chr11: 55,324,355-55,421,262 OR4A16, OR4A15, 3 more genes
    nsv5268942copy number variation1nstd204human GRCh38.p13 chr11: 55,365,536-55,372,949 , GRCh37.p13 chr11: 55,133,012-55,140,425 OR4A15
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