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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939576copy number variation1nstd209human GRCh38 chr20: 5,180,378-5,181,072 , GRCh37.p13 chr20: 5,161,024-5,161,718 CDS2
    nsv5720078mobile element insertion1nstd211human GRCh38 chr20: 5,159,485-5,159,485 , GRCh37.p13 chr20: 5,140,131-5,140,131 CDS2
    nsv5714328mobile element insertion1nstd211human GRCh38 chr20: 5,170,228-5,170,228 , GRCh37.p13 chr20: 5,150,874-5,150,874 CDS2
    nsv5546589insertion1nstd206human GRCh38 chr20: 5,168,274-5,168,277 , GRCh37.p13 chr20: 5,148,920-5,148,923 CDS2
    nsv5526095copy number variation1nstd206human GRCh38 chr20: 5,180,379-5,181,073 , GRCh37.p13 chr20: 5,161,025-5,161,719 CDS2
    nsv5427882mobile element insertion1nstd206human GRCh38 chr20: 5,170,228-5,170,279 , GRCh37.p13 chr20: 5,150,874-5,150,925 CDS2
    nsv5365898translocation1nstd200human GRCh38 chr20: 5,175,957-5,175,957 , GRCh38 chr20: 5,169,188-5,169,188 , GRCh37.p13 chr20: 5,156,603-5,156,603 , GRCh37.p13 chr20: 5,149,834-5,149,834 CDS2
    nsv5360028translocation1nstd200human GRCh38 chr20: 5,181,073-5,181,073 , GRCh38 chr20: 5,180,379-5,180,379 , GRCh37.p13 chr20: 5,161,719-5,161,719 , GRCh37.p13 chr20: 5,161,025-5,161,025 CDS2
    nsv5337177translocation1nstd200human GRCh37 chr20: 5,104,566-5,104,566 , GRCh37 chr20: 5,108,845-5,108,845 , GRCh38.p12 chr20: 5,123,920-5,123,920 , GRCh38.p12 chr20: 5,128,199-5,128,199 CDS2, PCNA
    nsv5332037translocation1nstd200human GRCh37 chr20: 5,161,719-5,161,719 , GRCh37 chr20: 5,161,025-5,161,025 , GRCh38.p12 chr20: 5,181,073-5,181,073 , GRCh38.p12 chr20: 5,180,379-5,180,379 CDS2
    nsv5328049copy number variation1nstd204human GRCh38.p13 chr20: 5,133,297-5,133,575 , GRCh37.p13 chr20: 5,113,943-5,114,221 CDS2
    nsv5287442copy number variation1nstd204human GRCh38.p13 chr20: 5,032,301-5,164,000 , GRCh37.p13 chr20: 5,012,947-5,144,646 PCNA-AS1, CDS2, 3 more genes
    nsv5185727mobile element insertion1nstd203human GRCh38 chr20: 5,160,877-5,160,896 , GRCh37.p13 chr20: 5,141,523-5,141,542 CDS2
    nsv5177140mobile element insertion1nstd203human GRCh38 chr20: 5,163,408-5,163,445 , GRCh37.p13 chr20: 5,144,054-5,144,091 CDS2
    nsv5175087mobile element insertion1nstd203human GRCh38 chr20: 5,125,527-5,125,543 , GRCh37.p13 chr20: 5,106,173-5,106,189 CDS2, PCNA
    nsv5171909mobile element insertion1nstd203human GRCh38 chr20: 5,168,260-5,168,274 , GRCh37.p13 chr20: 5,148,906-5,148,920 CDS2
    nsv5033561inversion1nstd200human GRCh38 chr20: 3,693,712-5,966,244 , GRCh37.p13 chr20: 3,674,359-5,946,890 , LOC107985411, 53 more genes
    nsv5025094copy number variation1nstd200human GRCh38 chr20: 5,177,667-5,230,569 , GRCh37.p13 chr20: 5,158,313-5,211,215 CDS2
    nsv5012313copy number variation1nstd200human GRCh38 chr20: 5,185,489-5,191,917 , GRCh37.p13 chr20: 5,166,135-5,172,563 CDS2
    nsv5012312copy number variation1nstd200human GRCh38 chr20: 5,140,984-5,143,017 , GRCh37.p13 chr20: 5,121,630-5,123,663 CDS2
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