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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128117copy number variation1nstd186human GRCh37 chr20: 35,264,591-35,264,845 , GRCh38.p12 chr20: 36,636,188-36,636,442 SLA2
    nsv5975262insertion1nstd209human GRCh38 chr20: 36,642,163-36,642,163 , GRCh37.p13 chr20: 35,270,566-35,270,566 SLA2
    nsv5965797copy number variation1nstd209human GRCh38 chr20: 36,637,171-36,637,221 , GRCh37.p13 chr20: 35,265,574-35,265,624 SLA2
    nsv5953998copy number variation1nstd209human GRCh38 chr20: 36,636,146-36,636,675 , GRCh37.p13 chr20: 35,264,549-35,265,078 SLA2
    nsv5667973insertion1nstd207human GRCh38 chr20: 36,642,167-36,642,167 , GRCh37.p13 chr20: 35,270,570-35,270,570 SLA2
    nsv5589599copy number variation1nstd207human GRCh38 chr20: 36,636,253-36,636,442 , GRCh37.p13 chr20: 35,264,656-35,264,845 SLA2
    nsv5560305sequence alteration1nstd206human GRCh38 chr20: 36,507,286-36,660,208 , GRCh37.p13 chr20: 35,135,689-35,288,611 , MYL9, 8 more genes
    nsv5530783copy number variation1nstd206human GRCh38 chr20: 36,636,188-36,636,442 , GRCh37.p13 chr20: 35,264,591-35,264,845 SLA2
    nsv5028495copy number variation1nstd200human GRCh38 chr20: 36,620,323-36,621,065 , GRCh37.p13 chr20: 35,248,726-35,249,468 SLA2, HNRNPA3P2
    nsv5028494copy number variation1nstd200human GRCh38 chr20: 36,618,155-36,621,540 , GRCh37.p13 chr20: 35,246,558-35,249,943 SLA2, HNRNPA3P2
    nsv5028493copy number variation1nstd200human GRCh38 chr20: 36,617,970-36,620,132 , GRCh37.p13 chr20: 35,246,373-35,248,535 SLA2, HNRNPA3P2
    nsv5028492copy number variation1nstd200human GRCh38 chr20: 36,617,861-36,619,458 , GRCh37.p13 chr20: 35,246,264-35,247,861 SLA2, HNRNPA3P2
    nsv5028491copy number variation1nstd200human GRCh38 chr20: 36,610,637-36,610,716 , GRCh37.p13 chr20: 35,239,040-35,239,119 TGIF2-RAB5IF, RAB5IF, 1 more genes
    nsv5025559copy number variation1nstd200human GRCh38 chr20: 36,619,933-36,669,345 , GRCh37.p13 chr20: 35,248,336-35,297,748 NDRG3, SLA2, 1 more genes
    nsv5025558copy number variation1nstd200human GRCh38 chr20: 36,607,389-36,620,929 , GRCh37.p13 chr20: 35,235,792-35,249,332 TGIF2-RAB5IF, HNRNPA3P2, 2 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868755copy number variation1nstd200human GRCh37 chr20: 35,264,586-35,265,083 , GRCh38.p12 chr20: 36,636,183-36,636,680 SLA2
    nsv4868754copy number variation1nstd200human GRCh37 chr20: 35,246,373-35,248,535 , GRCh38.p12 chr20: 36,617,970-36,620,132 SLA2, HNRNPA3P2
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