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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147759copy number variation1nstd232human GRCh37.p13 chr11: 1,775,131-1,775,222 , GRCh38.p12 chr11: 1,753,901-1,753,992 CTSD
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093927copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,785,002-1,785,089 , GRCh38.p12 chr11: 1,763,772-1,763,859 CTSD
    nsv7093926copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,774,733-2,019,125 , GRCh38.p12 chr11: 1,753,503-1,997,895 LINC01219, MIR7847, 16 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
    nsv7093246copy number variation1nstd102humanLikely benign GRCh37 chr11: 1,774,957-1,775,020 , GRCh38 chr11: 1,753,727-1,753,790 CTSD
    nsv7075432inversion1nstd229human GRCh38 chr11: 1,762,970-1,788,717 , GRCh37.p13 chr11: 1,784,200-1,809,947 CTSD, LOC105376517
    nsv7061927inversion1nstd229human GRCh38 chr11: 1,707,646-1,896,713 , GRCh37.p13 chr11: 1,728,876-1,917,943 MIR4298, LOC390029, 10 more genes
    nsv6915480copy number variation1nstd229human GRCh38 chr11: 1,735,811-1,821,007 , GRCh37.p13 chr11: 1,757,041-1,842,237 CTSD, IFITM10, 3 more genes
    nsv6903219copy number variation1nstd229human GRCh38 chr11: 1,755,030-1,757,322 , GRCh37.p13 chr11: 1,776,260-1,778,552 CTSD
    nsv6899093copy number variation1nstd229human GRCh38 chr11: 1,753,221-1,783,477 , GRCh37.p13 chr11: 1,774,451-1,804,707 LOC105376517, CTSD
    nsv6888081copy number variation1nstd229human GRCh38 chr11: 1,727,950-1,781,336 , GRCh37.p13 chr11: 1,749,180-1,802,566 CTSD, LOC105376517, 1 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
    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
    nsv6620716copy number variation1nstd224human GRCh37 chr11: 1,769,085-1,849,354 , GRCh38.p12 chr11: 1,747,855-1,828,124 CTSD, SYT8, 4 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
    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
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