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Items: 1 to 20 of 87

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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
    nsv7063495inversion1nstd229human GRCh38 chr11: 5,016,392-5,387,994 , GRCh37.p13 chr11: 5,037,622-5,409,224 OR51M1, OR52J2P, 29 more genes
    nsv7060711inversion1nstd229human GRCh38 chr11: 5,052,261-5,434,559 , GRCh37.p13 chr11: 5,073,491-5,455,789 HBD, OR52S1P, 29 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
    nsv6916243copy number variation1nstd229human GRCh38 chr11: 5,384,011-5,393,131 , GRCh37.p13 chr11: 5,405,241-5,414,361 OR51B5, OR51M1
    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
    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
    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
    nsv6621246copy number variation1nstd224human GRCh37 chr11: 5,372,751-5,444,353 , GRCh38.p12 chr11: 5,351,521-5,423,123 OR51J1, OR51B5, 5 more genes
    nsv6436221copy number variation1nstd223human GRCh38 chr11: 5,301,605-5,397,946 , GRCh37.p13 chr11: 5,322,835-5,419,176 OR51B4, OR51B3P, 7 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
    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
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4612348copy number variation1nstd183human GRCh37 chr11: 5,328,528-5,642,684 , GRCh38.p12 chr11: 5,307,298-5,621,454 OR51B3P, OR51I2, 27 more genes
    nsv4609693copy number variation1nstd183human GRCh37 chr11: 5,409,825-5,412,586 , GRCh38.p12 chr11: 5,388,595-5,391,356 OR51M1, OR51B5
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