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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6917043copy number variation1nstd229human GRCh38 chr11: 4,998,698-5,001,078 , GRCh37.p13 chr11: 5,019,928-5,022,308 OR51L1
    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
    nsv6905945copy number variation1nstd229human GRCh38 chr11: 4,976,115-5,005,604 , GRCh37.p13 chr11: 4,997,345-5,026,834 MMP26, OR51L1
    nsv6905649copy number variation1nstd229human GRCh38 chr11: 4,998,884-4,999,512 , GRCh37.p13 chr11: 5,020,114-5,020,742 OR51L1
    nsv6903103copy number variation1nstd229human GRCh38 chr11: 4,994,397-5,020,355 , GRCh37.p13 chr11: 5,015,627-5,041,585 OR51L1, OR51P1P
    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
    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
    nsv6450577copy number variation1nstd223human GRCh38 chr11: 4,619,075-5,268,953 , GRCh37.p13 chr11: 4,640,305-5,290,183 OR52J1P, OR51F2, 50 more genes
    nsv6444564copy number variation1nstd223human GRCh38 chr11: 4,976,201-5,005,600 , GRCh37.p13 chr11: 4,997,431-5,026,830 MMP26, OR51L1
    nsv6439692copy number variation1nstd223human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51S1, OR51F1, 39 more genes
    nsv6437793copy number variation1nstd223human GRCh38 chr11: 4,997,725-4,999,937 , GRCh37.p13 chr11: 5,018,955-5,021,167 OR51L1
    nsv6436703copy number variation1nstd223human GRCh38 chr11: 4,998,698-5,001,074 , GRCh37.p13 chr11: 5,019,928-5,022,304 OR51L1
    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
    nsv6291043copy number variation1nstd102humanLikely benign GRCh37 chr11: 4,937,852-5,037,488 , GRCh38.p12 chr11: 4,916,622-5,016,258 MMP26, OR51P1P, 6 more genes
    nsv6132106copy number variation1nstd213human GRCh37 chr11: 4,510,000-5,300,001 , GRCh38.p12 chr11: 4,488,770-5,278,771 HBB, HBBP1, 57 more genes
    nsv4977986copy number variation1nstd200human GRCh38 chr11: 4,997,725-4,999,937 , GRCh37.p13 chr11: 5,018,955-5,021,167 OR51L1
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