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Items: 1 to 20 of 290

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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
    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
    nsv6914504copy number variation1nstd229human GRCh38 chr11: 3,643,267-3,643,549 , GRCh37.p13 chr11: 3,664,497-3,664,779 ART1
    nsv6911991copy number variation1nstd229human GRCh38 chr11: 3,523,909-3,742,223 , GRCh37.p13 chr11: 3,545,139-3,763,453 OR7E117P, ART1, 11 more genes
    nsv6911777copy number variation1nstd229human GRCh38 chr11: 3,639,889-3,645,377 , GRCh37.p13 chr11: 3,661,119-3,666,607 ART5, ART1
    nsv6899954copy number variation1nstd229human GRCh38 chr11: 3,648,594-3,648,655 , GRCh37.p13 chr11: 3,669,824-3,669,885 ART1
    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
    nsv6452909copy number variation1nstd223human GRCh38 chr11: 3,662,093-3,669,077 , GRCh37.p13 chr11: 3,683,323-3,690,307 CHRNA10, ART1
    nsv6446487copy number variation1nstd223human GRCh38 chr11: 3,598,372-3,731,272 , GRCh37.p13 chr11: 3,619,602-3,752,502 ART1, NUP98, 6 more genes
    nsv6439780copy number variation1nstd223human GRCh38 chr11: 3,562,701-3,708,100 , GRCh37.p13 chr11: 3,583,931-3,729,330 ART5, OR7E117P, 7 more genes
    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
    nsv6435646copy number variation1nstd223human GRCh38 chr11: 3,643,250-3,643,549 , GRCh37.p13 chr11: 3,664,480-3,664,779 ART1
    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
    nsv6274658copy number variation1nstd214human GRCh38 chr11: 3,653,797-3,653,920 , GRCh37.p13 chr11: 3,675,027-3,675,150 ART1
    nsv6271281copy number variation1nstd214human GRCh38 chr11: 3,654,677-3,654,796 , GRCh37.p13 chr11: 3,675,907-3,676,026 ART1
    nsv6271255copy number variation1nstd214human GRCh38 chr11: 3,663,025-3,663,075 , GRCh37.p13 chr11: 3,684,255-3,684,305 ART1
    nsv6271179copy number variation1nstd214human GRCh38 chr11: 3,653,822-3,653,946 , GRCh37.p13 chr11: 3,675,052-3,675,176 ART1
    nsv6200532copy number variation1nstd214human GRCh38 chr11: 3,663,033-3,663,093 , GRCh37.p13 chr11: 3,684,263-3,684,323 ART1
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