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Items: 1 to 20 of 354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116630mobile element insertion1nstd186human GRCh37 chr20: 32,831,297-32,831,348 , GRCh38.p12 chr20: 34,243,491-34,243,542 ASIP, AHCY
    nsv5976620insertion1nstd209human GRCh38 chr20: 34,235,913-34,235,913 , GRCh37.p13 chr20: 32,823,719-32,823,719 AHCY, ASIP
    nsv5967161copy number variation1nstd209human GRCh38 chr20: 34,274,782-34,276,679 , GRCh37.p13 chr20: 32,862,588-32,864,485 AHCY
    nsv5956119copy number variation1nstd209human GRCh38 chr20: 34,266,071-34,266,389 , GRCh37.p13 chr20: 32,853,877-32,854,195 AHCY, ASIP
    nsv5952950copy number variation1nstd209human GRCh38 chr20: 34,143,842-34,843,201 , GRCh37.p13 chr20: 32,731,648-33,431,004 , AHCY, 15 more genes
    nsv5873913copy number variation1nstd209human GRCh38 chr20: 34,274,759-34,276,658 , GRCh37.p13 chr20: 32,862,565-32,864,464 AHCY
    nsv5707360mobile element insertion2nstd211human GRCh38 chr20: 34,243,491-34,243,491 , GRCh37.p13 chr20: 32,831,297-32,831,297 ASIP, AHCY
    nsv5671386insertion1nstd207human GRCh38 chr20: 34,243,476-34,243,476 , GRCh37.p13 chr20: 32,831,282-32,831,282 ASIP, AHCY
    nsv5670614insertion1nstd207human GRCh38 chr20: 34,235,952-34,235,952 , GRCh37.p13 chr20: 32,823,758-32,823,758 AHCY, ASIP
    nsv5548327insertion1nstd206human GRCh38 chr20: 34,258,154-34,258,204 , GRCh37.p13 chr20: 32,845,960-32,846,010 ASIP, AHCY
    nsv5519676copy number variation1nstd206human GRCh38 chr20: 34,290,940-34,291,418 , GRCh37.p13 chr20: 32,878,746-32,879,224 AHCY
    nsv5518568copy number variation1nstd206human GRCh38 chr20: 34,291,533-34,292,356 , GRCh37.p13 chr20: 32,879,339-32,880,162 AHCY
    nsv5517247copy number variation1nstd206human GRCh38 chr20: 34,258,684-34,258,753 , GRCh37.p13 chr20: 32,846,490-32,846,559 AHCY, ASIP
    nsv5516737copy number variation1nstd206human GRCh38 chr20: 34,285,636-34,290,328 , GRCh37.p13 chr20: 32,873,442-32,878,134 AHCY
    nsv5414909mobile element insertion1nstd206human GRCh38 chr20: 34,243,491-34,243,542 , GRCh37.p13 chr20: 32,831,297-32,831,348 ASIP, AHCY
    nsv5284216copy number variation1nstd204human GRCh38.p13 chr20: 34,272,001-34,435,200 , GRCh37.p13 chr20: 32,859,807-33,023,006 , ITCH, 2 more genes
    nsv5196940mobile element insertion1nstd203human GRCh38 chr20: 34,240,215-34,240,228 , GRCh37.p13 chr20: 32,828,021-32,828,034 ASIP, AHCY
    nsv5185698mobile element insertion1nstd203human GRCh38 chr20: 34,300,306-34,300,316 , GRCh37.p13 chr20: 32,888,112-32,888,122 AHCY
    nsv5180603mobile element insertion1nstd203human GRCh38 chr20: 34,306,662-34,306,678 , GRCh37.p13 chr20: 32,894,468-32,894,484 AHCY
    nsv5176564mobile element insertion1nstd203human GRCh38 chr20: 34,247,300-34,247,350 , GRCh37.p13 chr20: 32,835,106-32,835,156 AHCY, ASIP
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