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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6621113copy number variation1nstd224human GRCh37 chr11: 55,171,027-55,406,762 , GRCh38.p12 chr11: 55,403,551-55,639,286 OR4P4, OR4C14P, 11 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
    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
    nsv6194612copy number variation1nstd214human GRCh38 chr11: 55,511,195-55,511,266 , GRCh37.p13 chr11: 55,278,671-55,278,742 OR4C1P
    nsv6132181copy number variation1nstd213human GRCh37 chr11: 55,140,000-55,330,001 , GRCh38.p12 chr11: 55,372,524-55,562,525 OR4C14P, OR4A14P, 9 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 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
    nsv5910830copy number variation1nstd209human GRCh38 chr11: 55,484,440-55,541,014 , GRCh37.p13 chr11: 55,251,916-55,308,490 OR4C1P, OR4C14P, 1 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
    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
    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
    nsv5263389copy number variation1nstd204human GRCh37.p13 chr11: 55,201,277-55,364,476 , GRCh38.p13 chr11: 55,433,801-55,597,000 OR4C1P, OR4C15, 7 more genes
    nsv5190886mobile element insertion1nstd203human GRCh38 chr11: 55,508,261-55,508,277 , GRCh37.p13 chr11: 55,275,737-55,275,753 OR4C1P
    nsv5039221inversion1nstd200human GRCh38 chr11: 55,481,910-55,566,654 , GRCh37.p13 chr11: 55,249,386-55,334,130 OR4C1P, OR4C15, 2 more genes
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