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Items: 1 to 20 of 113

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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
    nsv6916174copy number variation1nstd229human GRCh38 chr11: 5,447,942-5,467,900 , GRCh37.p13 chr11: 5,469,172-5,489,130 OR51B5, OR51A10P, 1 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
    nsv6904962copy number variation1nstd229human GRCh38 chr11: 5,412,518-5,475,696 , GRCh37.p13 chr11: 5,433,748-5,496,926 OR51A10P, OR51B5, 4 more genes
    nsv6900302copy number variation1nstd229human GRCh38 chr11: 5,409,708-5,471,203 , GRCh37.p13 chr11: 5,430,938-5,492,433 OR51A10P, OR51K1P, 4 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
    nsv6621247copy number variation2nstd224human GRCh37 chr11: 5,431,986-5,491,183 , GRCh38.p12 chr11: 5,410,756-5,469,953 OR51K1P, OR51A10P, 4 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
    nsv6033294copy number variation1nstd212human GRCh37.p13 chr11: 5,430,938-5,492,430 , GRCh38 chr11: 5,409,708-5,471,200 OR51K1P, OR51A10P, 4 more genes
    nsv5495573copy number variation1nstd206human GRCh38 chr11: 5,409,708-5,471,199 , GRCh37.p13 chr11: 5,430,938-5,492,429 OR51K1P, OR51A10P, 4 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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