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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146685copy number variation1nstd232human GRCh37.p13 chr11: 1,707,961-1,708,029 , GRCh38.p12 chr11: 1,686,731-1,686,799 LINC02708
    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
    nsv6889780copy number variation1nstd229human GRCh38 chr11: 1,677,298-1,698,963 , GRCh37.p13 chr11: 1,698,528-1,720,193 FAM99B, KRTAP5-6, 1 more genes
    nsv6888109copy number variation1nstd229human GRCh38 chr11: 1,558,735-1,701,768 , GRCh37.p13 chr11: 1,579,965-1,722,998 KRTAP5-4, FAM99A, 9 more genes
    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
    nsv6879718copy number variation1nstd229human GRCh38 chr11: 1,203,314-1,714,253 , GRCh37.p13 chr11: 1,224,544-1,735,483 KRTAP5-3, KRTAP5-2, 17 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
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 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
    nsv6620713copy number variation1nstd224human GRCh37 chr11: 1,629,693-1,881,256 , GRCh38.p12 chr11: 1,608,463-1,860,026 , GRCh38.p12 chr11|NT_187657.1: 85,016-214,625 TNNI2, KRTAP5-3, 15 more genes
    nsv6453107copy number variation1nstd223human GRCh38 chr11: 1,685,001-1,693,200 , GRCh37.p13 chr11: 1,706,231-1,714,430 LINC02708, FAM99B
    nsv6449853copy number variation1nstd223human GRCh38 chr11: 1,686,682-1,687,092 , GRCh37.p13 chr11: 1,707,912-1,708,322 LINC02708
    nsv6440640copy number variation1nstd223human GRCh38 chr11: 1,687,901-1,689,200 , GRCh37.p13 chr11: 1,709,131-1,710,430 LINC02708
    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
    nsv6315550copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,621,232-2,228,572 , GRCh38.p12 chr11: 1,600,002-2,207,342 IGF2-AS, SNORD131, 31 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
    nsv6308322insertion1nstd186human GRCh37 chr11: 1,708,033-1,708,118 , GRCh38.p12 chr11: 1,686,803-1,686,888 LINC02708
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6271941copy number variation1nstd214human GRCh38 chr11: 1,686,731-1,686,799 , GRCh37.p13 chr11: 1,707,961-1,708,029 LINC02708
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