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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093761copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489 TOLLIP-DT, KRTAP5-6, 58 more genes
    nsv6917469copy number variation1nstd229human GRCh38 chr11: 2,867,748-2,894,423 , GRCh37.p13 chr11: 2,888,978-2,915,653 SLC22A18AS, KCNQ1DN, 1 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
    nsv6914993copy number variation1nstd229human GRCh38 chr11: 2,897,103-2,902,890 , GRCh37.p13 chr11: 2,918,333-2,924,120 SLC22A18AS, SLC22A18
    nsv6913592copy number variation1nstd229human GRCh38 chr11: 2,838,203-2,957,732 , GRCh37.p13 chr11: 2,859,433-2,978,962 KCNQ1, PHLDA2, 6 more genes
    nsv6910793copy number variation1nstd229human GRCh38 chr11: 2,903,007-2,912,143 , GRCh37.p13 chr11: 2,924,237-2,933,373 SLC22A18AS, SLC22A18
    nsv6885276copy number variation1nstd229human GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693 KRTAP5-1, MIR675, 69 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
    nsv6440893copy number variation1nstd223human GRCh38 chr11: 2,897,100-2,902,889 , GRCh37.p13 chr11: 2,918,330-2,924,119 SLC22A18, SLC22A18AS
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
    nsv6315544copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,314,240-2,915,570 , GRCh38.p12 chr11: 2,293,010-2,894,340 COX6CP18, SLC22A18AS, 14 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
    nsv6309362copy number variation1nstd102humanPathogenic GRCh37 chr11: 2,905,228-2,906,725 , GRCh38.p12 chr11: 2,883,998-2,885,495 , GRCh38.p12 chr11|NT_187585.1: 116,177-117,705 CDKN1C, SLC22A18AS, 1 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
    nsv6204969copy number variation1nstd214human GRCh38 chr11: 2,897,837-2,897,905 , GRCh37.p13 chr11: 2,919,067-2,919,135 SLC22A18AS, SLC22A18
    nsv6203201copy number variation1nstd214human GRCh38 chr11: 2,897,866-2,897,925 , GRCh37.p13 chr11: 2,919,096-2,919,155 SLC22A18AS, SLC22A18
    nsv6200721copy number variation1nstd214human GRCh38 chr11: 2,897,823-2,897,891 , GRCh37.p13 chr11: 2,919,053-2,919,121 SLC22A18, SLC22A18AS
    nsv6198480copy number variation1nstd214human GRCh38 chr11: 2,897,917-2,897,984 , GRCh37.p13 chr11: 2,919,147-2,919,214 SLC22A18, SLC22A18AS
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