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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5878643copy number variation1nstd209human GRCh38 chr20: 33,822,792-33,824,291 , GRCh37.p13 chr20: 32,410,598-32,412,097 CHMP4B
    nsv5713228mobile element insertion1nstd211human GRCh38 chr20: 33,831,745-33,831,745 , GRCh37.p13 chr20: 32,419,551-32,419,551 CHMP4B
    nsv5536419insertion1nstd206human GRCh38 chr20: 33,831,745-33,831,782 , GRCh37.p13 chr20: 32,419,551-32,419,588 CHMP4B
    nsv5194045mobile element insertion1nstd203human GRCh38 chr20: 33,809,712-33,809,728 , GRCh37.p13 chr20: 32,397,518-32,397,534 CHMP4B, ZNF341-AS1
    nsv5166591mobile element insertion1nstd203human GRCh38 chr20: 33,831,731-33,831,745 , GRCh37.p13 chr20: 32,419,537-32,419,551 CHMP4B
    nsv5025531copy number variation1nstd200human GRCh38 chr20: 33,814,902-33,823,953 , GRCh37.p13 chr20: 32,402,708-32,411,759 CHMP4B
    nsv5022402copy number variation1nstd200human GRCh38 chr20: 33,824,662-33,830,369 , GRCh37.p13 chr20: 32,412,468-32,418,175 CHMP4B
    nsv5022401copy number variation1nstd200human GRCh38 chr20: 33,822,414-33,823,753 , GRCh37.p13 chr20: 32,410,220-32,411,559 CHMP4B
    nsv5022400copy number variation1nstd200human GRCh38 chr20: 33,807,136-33,809,636 , GRCh37.p13 chr20: 32,394,942-32,397,442 CHMP4B, ZNF341-AS1
    nsv5022399copy number variation1nstd200human GRCh38 chr20: 33,806,011-33,809,487 , GRCh37.p13 chr20: 32,393,817-32,397,293 CHMP4B, ZNF341-AS1
    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
    nsv4868635copy number variation1nstd200human GRCh37 chr20: 32,412,468-32,418,175 , GRCh38.p12 chr20: 33,824,662-33,830,369 CHMP4B
    nsv4868634copy number variation1nstd200human GRCh37 chr20: 32,410,220-32,411,559 , GRCh38.p12 chr20: 33,822,414-33,823,753 CHMP4B
    nsv4868633copy number variation1nstd200human GRCh37 chr20: 32,394,942-32,397,442 , GRCh38.p12 chr20: 33,807,136-33,809,636 CHMP4B, ZNF341-AS1
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4865535copy number variation1nstd200human GRCh37 chr20: 32,357,542-32,432,385 , GRCh38.p12 chr20: 33,769,736-33,844,579 CHMP4B, ZNF341-AS1, 1 more genes
    nsv4676132copy number variation1nstd102humanUncertain significance GRCh37 chr20: 31,966,407-33,169,058 , GRCh38.p12 chr20: 33,378,601-34,581,254 MAP1LC3A, PXMP4, 28 more genes
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