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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957418copy number variation1nstd209human GRCh38 chr20: 34,079,430-34,079,495 , GRCh37.p13 chr20: 32,667,236-32,667,301 RALY
    nsv5954434copy number variation1nstd209human GRCh38 chr20: 34,044,011-34,048,119 , GRCh37.p13 chr20: 32,631,817-32,635,925 RALY, MIR4755
    nsv5884085copy number variation1nstd209human GRCh38 chr20: 34,043,991-34,047,590 , GRCh37.p13 chr20: 32,631,797-32,635,396 MIR4755, RALY
    nsv5713534mobile element insertion1nstd211human GRCh38 chr20: 34,025,899-34,025,899 , GRCh37.p13 chr20: 32,613,705-32,613,705 RALY
    nsv5708946mobile element insertion1nstd211human GRCh38 chr20: 34,025,949-34,025,949 , GRCh37.p13 chr20: 32,613,755-32,613,755 RALY
    nsv5533344copy number variation1nstd206human GRCh38 chr20: 34,048,916-34,049,168 , GRCh37.p13 chr20: 32,636,722-32,636,974 MIR4755, RALY
    nsv5517566copy number variation1nstd206human GRCh38 chr20: 34,035,121-34,035,231 , GRCh37.p13 chr20: 32,622,927-32,623,037 RALY
    nsv5515847copy number variation1nstd206human GRCh38 chr20: 34,043,147-34,043,197 , GRCh37.p13 chr20: 32,630,953-32,631,003 RALY
    nsv5366091translocation1nstd200human GRCh38 chr20: 34,040,204-34,040,204 , GRCh38 chr20: 34,040,846-34,040,846 , GRCh37.p13 chr20: 32,628,010-32,628,010 , GRCh37.p13 chr20: 32,628,652-32,628,652 RALY
    nsv5343767translocation1nstd200human GRCh37 chr20: 32,667,236-32,667,236 , GRCh37 chr20: 32,667,302-32,667,302 , GRCh38.p12 chr20: 34,079,496-34,079,496 , GRCh38.p12 chr20: 34,079,430-34,079,430 RALY
    nsv5342957translocation1nstd200human GRCh37 chr20: 32,584,445-32,584,445 , GRCh37 chr20: 32,583,193-32,583,193 , GRCh38.p12 chr20: 33,996,639-33,996,639 , GRCh38.p12 chr20: 33,995,387-33,995,387 RALY
    nsv5337686translocation1nstd200human GRCh37 chr20: 32,584,478-32,584,478 , GRCh37 chr20: 32,583,377-32,583,377 , GRCh38.p12 chr20: 33,996,672-33,996,672 , GRCh38.p12 chr20: 33,995,571-33,995,571 RALY
    nsv5332886translocation1nstd200human GRCh37 chr20: 32,628,010-32,628,010 , GRCh37 chr20: 32,628,652-32,628,652 , GRCh38.p12 chr20: 34,040,204-34,040,204 , GRCh38.p12 chr20: 34,040,846-34,040,846 RALY
    nsv5025533copy number variation1nstd200human GRCh38 chr20: 34,080,540-34,080,992 , GRCh37.p13 chr20: 32,668,346-32,668,798 RALY
    nsv5025532copy number variation1nstd200human GRCh38 chr20: 34,031,846-34,032,526 , GRCh37.p13 chr20: 32,619,652-32,620,332 RALY
    nsv5022411copy number variation1nstd200human GRCh38 chr20: 34,048,937-34,049,148 , GRCh37.p13 chr20: 32,636,743-32,636,954 MIR4755, RALY
    nsv5022410copy number variation1nstd200human GRCh38 chr20: 34,043,598-34,045,004 , GRCh37.p13 chr20: 32,631,404-32,632,810 RALY
    nsv5022409copy number variation1nstd200human GRCh38 chr20: 34,022,937-34,031,228 , GRCh37.p13 chr20: 32,610,743-32,619,034 RALY
    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
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