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Items: 1 to 20 of 129

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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
    nsv6917454copy number variation1nstd229human GRCh38 chr11: 4,933,642-5,211,794 , GRCh37.p13 chr11: 4,954,872-5,233,024 OR51A3P, OR52J2P, 18 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
    nsv6914195copy number variation1nstd229human GRCh38 chr11: 5,091,061-5,156,717 , GRCh37.p13 chr11: 5,112,291-5,177,947 OR52E3P, OR52A1, 3 more genes
    nsv6913447copy number variation1nstd229human GRCh38 chr11: 5,075,892-5,199,228 , GRCh37.p13 chr11: 5,097,122-5,220,458 OR51A1P, OR52S1P, 7 more genes
    nsv6912684copy number variation1nstd229human GRCh38 chr11: 5,123,827-5,194,482 , GRCh37.p13 chr11: 5,145,057-5,215,712 OR52Z1P, OR51A1P, 2 more genes
    nsv6912161copy number variation1nstd229human GRCh38 chr11: 5,110,501-5,199,600 , GRCh37.p13 chr11: 5,131,731-5,220,830 OR51A1P, OR52Z1P, 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
    nsv6905451copy number variation1nstd229human GRCh38 chr11: 5,091,001-5,156,700 , GRCh37.p13 chr11: 5,112,231-5,177,930 OR52E3P, OR52A5, 3 more genes
    nsv6903025copy number variation1nstd229human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51V1, OR51L1, 39 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
    nsv6902288copy number variation1nstd229human GRCh38 chr11: 5,132,186-5,154,092 , GRCh37.p13 chr11: 5,153,416-5,175,322 OR52A5, OR52A1
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 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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