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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115442mobile element insertion1nstd186human GRCh37 chr20: 62,504,414-62,504,465 , GRCh38.p12 chr20: 63,873,061-63,873,112 TPD52L2
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5973388insertion1nstd209human GRCh38 chr20: 63,873,048-63,873,048 , GRCh37.p13 chr20: 62,504,401-62,504,401 TPD52L2
    nsv5949709copy number variation1nstd209human GRCh38 chr20: 63,873,061-63,873,206 , GRCh37.p13 chr20: 62,504,414-62,504,559 TPD52L2
    nsv5701950mobile element insertion2nstd211human GRCh38 chr20: 63,873,061-63,873,061 , GRCh37.p13 chr20: 62,504,414-62,504,414 TPD52L2
    nsv5668813insertion1nstd207human GRCh38 chr20: 63,873,048-63,873,048 , GRCh37.p13 chr20: 62,504,401-62,504,401 TPD52L2
    nsv5585916copy number variation1nstd207human GRCh38 chr20: 63,880,003-63,880,122 , GRCh37.p13 chr20: 62,511,356-62,511,475 TPD52L2
    nsv5562694sequence alteration1nstd206human GRCh38 chr20: 63,525,502-63,937,515 , GRCh37.p13 chr20: 62,156,855-62,568,868 , STMN3, 26 more genes
    nsv5424656mobile element insertion1nstd206human GRCh38 chr20: 63,873,061-63,873,112 , GRCh37.p13 chr20: 62,504,414-62,504,465 TPD52L2
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5361890translocation1nstd200human GRCh38 chr20: 63,883,859-63,883,859 , GRCh38 chr3: 123,151,735-123,151,735 , GRCh37.p13 chr20: 62,515,212-62,515,212 , GRCh37.p13 chr3: 122,870,582-122,870,582 PDIA5, TPD52L2
    nsv5343608translocation1nstd200human GRCh37 chr3: 122,870,582-122,870,582 , GRCh37 chr20: 62,515,212-62,515,212 , GRCh38.p12 chr20: 63,883,859-63,883,859 , GRCh38.p12 chr3: 123,151,735-123,151,735 TPD52L2, PDIA5
    nsv5328502copy number variation1nstd204human GRCh37.p13 chr20: 62,431,525-62,501,332 , GRCh38.p13 chr20: 63,800,172-63,869,979 TPD52L2, ZBTB46, 4 more genes
    nsv5300305copy number variation1nstd204human GRCh38.p13 chr20: 63,873,927-63,877,758 , GRCh37.p13 chr20: 62,505,280-62,509,111 TPD52L2
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv5290859copy number variation1nstd204human GRCh37.p13 chr20: 62,431,554-62,501,353 , GRCh38.p13 chr20: 63,800,201-63,870,000 TPD52L2, ZBTB46, 4 more genes
    nsv5287268copy number variation1nstd204human GRCh38.p13 chr20: 63,850,201-63,880,500 , GRCh37.p13 chr20: 62,481,554-62,511,853 ABHD16B, TPD52L2, 1 more genes
    nsv5286918copy number variation1nstd204human GRCh38.p13 chr20: 63,836,601-63,964,800 , GRCh37.p13 chr20: 62,467,954-62,596,153 DNAJC5, C20orf181, 14 more genes
    nsv5284952copy number variation1nstd204human GRCh38.p13 chr20: 63,832,323-63,870,515 , GRCh37.p13 chr20: 62,463,676-62,501,868 ZBTB46, C20orf181, 3 more genes
    nsv5282963copy number variation1nstd204human GRCh38.p13 chr20: 63,863,001-64,088,600 , GRCh37.p13 chr20: 62,494,354-62,719,953 DNAJC5, RGS19, 22 more genes
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