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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5861270copy number variation2nstd209human GRCh38 chr11: 48,320,921-48,374,030 , GRCh37.p13 chr11: 48,342,473-48,395,582 OR4C4P, OR4C3, 1 more genes
    nsv5512026copy number variation1nstd206human GRCh38 chr11: 48,351,168-48,446,286 , GRCh37.p13 chr11: 48,372,720-48,467,838 OR4C5, OR4C10P, 2 more genes
    nsv5506322copy number variation1nstd206human GRCh38 chr11: 48,106,678-48,968,618 , GRCh37.p13 chr11: 48,128,230-48,990,170 , OR4X2, 24 more genes
    nsv5501574copy number variation1nstd206human GRCh38 chr11: 48,234,530-48,888,316 , GRCh37.p13 chr11: 48,256,082-48,909,868 OR4A45P, OR4A42P, 17 more genes
    nsv5393660mobile element deletion1nstd186human GRCh37 chr11: 48,367,528-48,373,693 , GRCh38.p12 chr11: 48,345,976-48,352,141 OR4C4P
    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
    nsv5317179copy number variation1nstd204human GRCh38.p13 chr11: 47,892,317-48,385,775 , GRCh37.p13 chr11: 47,913,869-48,407,327 LOC100287189, OR4C4P, 9 more genes
    nsv4984494copy number variation1nstd200human GRCh38 chr11: 48,292,745-48,346,480 , GRCh37.p13 chr11: 48,314,297-48,368,032 OR4C3, OR4C4P, 1 more genes
    nsv4984493copy number variation1nstd200human GRCh38 chr11: 48,234,530-48,888,316 , GRCh37.p13 chr11: 48,256,082-48,909,868 OR4C4P, OR4C9P, 17 more genes
    nsv4984491copy number variation1nstd200human GRCh38 chr11: 48,198,392-48,796,502 , GRCh37.p13 chr11: 48,219,944-48,818,054 OR4A45P, OR4B1, 19 more genes
    nsv4984490copy number variation1nstd200human GRCh38 chr11: 48,160,022-48,369,463 , GRCh37.p13 chr11: 48,181,574-48,391,015 OR4B2P, OR4C5, 7 more genes
    nsv4984489copy number variation1nstd200human GRCh38 chr11: 48,042,022-48,521,916 , GRCh37.p13 chr11: 48,063,574-48,543,468 OR4R1P, OR4A40P, 16 more genes
    nsv4971044copy number variation1nstd200human GRCh38 chr11: 48,262,250-48,381,485 , GRCh37.p13 chr11: 48,283,802-48,403,037 OR4C3, OR4X1, 3 more genes
    nsv4874046mobile element deletion1nstd200human GRCh37 chr11: 48,367,528-48,373,693 , GRCh38.p12 chr11: 48,345,976-48,352,141 OR4C4P
    nsv4848991copy number variation1nstd200human GRCh37 chr11: 48,366,790-48,366,888 , GRCh38.p12 chr11: 48,345,238-48,345,336 OR4C4P
    nsv4846031copy number variation1nstd200human GRCh37 chr11: 48,181,574-48,391,015 , GRCh38.p12 chr11: 48,160,022-48,369,463 PTPRJ, OR4B2P, 7 more genes
    nsv4842459copy number variation1nstd200human GRCh37 chr11: 47,914,073-48,407,132 , GRCh38.p12 chr11: 47,892,521-48,385,580 LOC100287189, OR4B1, 9 more genes
    nsv4829546copy number variation1nstd200human GRCh37 chr11: 48,256,082-48,909,868 , GRCh38.p12 chr11: 48,234,530-48,888,316 OR4A45P, OR4A48P, 17 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
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