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Items: 1 to 20 of 93

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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
    nsv7071479inversion1nstd229human GRCh38 chr11: 5,494,451-5,536,643 , GRCh37.p13 chr11: 5,515,681-5,557,873 UBQLNL, OR51B5, 3 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
    nsv6905596copy number variation1nstd229human GRCh38 chr11: 5,518,111-5,534,572 , GRCh37.p13 chr11: 5,539,341-5,555,802 OR52V1P, OLFM5P
    nsv6905560copy number variation1nstd229human GRCh38 chr11: 5,518,301-5,521,100 , GRCh37.p13 chr11: 5,539,531-5,542,330 OLFM5P
    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
    nsv6621114copy number variation1nstd224human GRCh37 chr11: 5,543,019-5,554,126 , GRCh38.p12 chr11: 5,521,789-5,532,896 OR52V1P, OLFM5P
    nsv6435653copy number variation1nstd223human GRCh38 chr11: 5,502,286-5,526,914 , GRCh37.p13 chr11: 5,523,516-5,548,144 UBQLN3, OR51B5, 3 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
    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
    nsv6283835insertion1nstd214human GRCh38 chr11: 5,519,887-5,519,887 , GRCh37.p13 chr11: 5,541,117-5,541,117 OLFM5P
    nsv5648690insertion1nstd207human GRCh38 chr11: 5,521,975-5,521,975 , GRCh37.p13 chr11: 5,543,205-5,543,205 OLFM5P
    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
    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
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