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Items: 1 to 20 of 183

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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
    nsv7136988copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 5,248,030-5,255,220 , GRCh38.p12 chr11: 5,226,800-5,233,990 HBB, HBD
    nsv7094088copy number variation1nstd102humanPathogenic GRCh37 chr11: 5,247,870-5,251,001 , GRCh38.p12 chr11: 5,226,640-5,229,771 HBB
    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
    nsv6917060copy number variation1nstd229human GRCh38 chr11: 5,112,883-5,231,359 , GRCh37.p13 chr11: 5,134,113-5,252,589 OR52A4P, HBB, 6 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
    nsv6915880copy number variation1nstd229human GRCh38 chr11: 5,144,392-5,237,243 , GRCh37.p13 chr11: 5,165,622-5,258,473 OR51A1P, HBD, 4 more genes
    nsv6908758copy number variation1nstd229human GRCh38 chr11: 5,101,702-5,241,698 , GRCh37.p13 chr11: 5,122,932-5,262,928 OR51A1P, HBD, 8 more genes
    nsv6907831copy number variation1nstd229human GRCh38 chr11: 5,201,647-5,229,059 , GRCh37.p13 chr11: 5,222,877-5,250,289 HBB
    nsv6906676copy number variation1nstd229human GRCh38 chr11: 5,153,222-5,238,139 , GRCh37.p13 chr11: 5,174,452-5,259,369 HBD, OR51A1P, 3 more genes
    nsv6904757copy number variation1nstd229human GRCh38 chr11: 5,167,007-5,239,653 , GRCh37.p13 chr11: 5,188,237-5,260,883 HBD, OR52Z1P, 3 more genes
    nsv6902995copy number variation1nstd229human GRCh38 chr11: 4,619,101-5,268,938 , GRCh37.p13 chr11: 4,640,331-5,290,168 OR51A9P, OR51F1, 50 more genes
    nsv6902251copy number variation1nstd229human GRCh38 chr11: 5,194,457-5,244,223 , GRCh37.p13 chr11: 5,215,687-5,265,453 OR51V1, HBB, 3 more genes
    nsv6899745copy number variation1nstd229human GRCh38 chr11: 5,212,723-5,253,494 , GRCh37.p13 chr11: 5,233,953-5,274,724 HBD, HBB, 4 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
    nsv6634463copy number variation1nstd102humanPathogenic GRCh37 chr11: 5,198,944-5,255,663 , GRCh38.p12 chr11: 5,177,714-5,234,433 OR51V1, HBB, 2 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6621245copy number variation1nstd224human GRCh37 chr11: 5,138,733-5,253,586 , GRCh38.p12 chr11: 5,117,503-5,232,356 HBB, HBD, 6 more genes
    nsv6620765copy number variation1nstd224human GRCh37 chr11: 5,138,733-5,249,570 , GRCh38.p12 chr11: 5,117,503-5,228,340 HBB, OR52A1, 5 more genes
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