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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    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
    nsv6910790copy number variation1nstd229human GRCh38 chr11: 5,368,252-5,542,054 , GRCh37.p13 chr11: 5,389,482-5,563,284 OR51K1P, OR51B5, 11 more genes
    nsv6908793copy number variation1nstd229human GRCh38 chr11: 5,477,750-5,505,828 , GRCh37.p13 chr11: 5,498,980-5,527,058 OR51B5, UBQLN3, 1 more genes
    nsv6898769copy number variation1nstd229human GRCh38 chr11: 5,442,003-5,689,638 , GRCh37.p13 chr11: 5,463,233-5,710,868 TRIM6, TRIM22, 19 more genes
    nsv6638042copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,361,272-5,660,023 , GRCh38.p12 chr11: 5,340,042-5,638,793 OR51A10P, OR52H2P, 24 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
    nsv6637653copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,439,244-5,570,043 , GRCh38.p12 chr11: 5,418,014-5,548,813 OLFM5P, UBQLN3, 10 more genes
    nsv6637234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,279,153-5,619,949 , GRCh38.p12 chr11: 5,257,923-5,598,719 OR51A10P, OR51B5, 29 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
    nsv6290806copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,373,646-5,519,671 , GRCh38.p12 chr11: 5,352,416-5,498,441 OR51Q1, OR51B6, 10 more genes
    nsv6290738copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,488,908-5,701,819 , GRCh38.p12 chr11: 5,467,678-5,680,589 UBQLN3, OLFM5P, 16 more genes
    nsv5506878copy number variation1nstd206human GRCh38 chr11: 5,464,000-5,676,000 , GRCh37.p13 chr11: 5,485,230-5,697,230 OR52V1P, HNRNPA1P53, 16 more genes
    nsv5242738copy number variation1nstd204human GRCh38.p13 chr11: 5,489,060-5,491,059 , GRCh37.p13 chr11: 5,510,290-5,512,289 OR52D1, OR51B5
    nsv4978008copy number variation1nstd200human GRCh38 chr11: 5,477,722-5,505,854 , GRCh37.p13 chr11: 5,498,952-5,527,084 OR51B5, OR52D1, 1 more genes
    nsv4847534copy number variation1nstd200human GRCh37 chr11: 5,498,977-5,527,057 , GRCh38.p12 chr11: 5,477,747-5,505,827 OR51B5, OR52D1, 1 more genes
    nsv4833520copy number variation1nstd200human GRCh37 chr11: 5,433,133-5,568,488 , GRCh38.p12 chr11: 5,411,903-5,547,258 OR51Q1, UBQLNL, 10 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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