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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928976copy number variation1nstd209human GRCh38 chr19: 36,022,253-36,026,653 , GRCh37.p13 chr19: 36,513,155-36,517,555 CLIP3, LOC101927572
    nsv5869355copy number variation1nstd209human GRCh38 chr19: 36,023,515-36,026,364 , GRCh37.p13 chr19: 36,514,417-36,517,266 CLIP3, LOC101927572
    nsv5531520copy number variation1nstd206human GRCh38 chr19: 36,029,513-36,044,516 , GRCh37.p13 chr19: 36,520,415-36,535,418 CLIP3, THAP8, 1 more genes
    nsv5528024copy number variation1nstd206human GRCh38 chr19: 36,018,020-36,084,516 , GRCh37.p13 chr19: 36,508,922-36,575,418 WDR62, RNY5P10, 3 more genes
    nsv5516454copy number variation1nstd206human GRCh38 chr19: 36,024,899-36,025,424 , GRCh37.p13 chr19: 36,515,801-36,516,326 LOC101927572, CLIP3
    nsv5289021copy number variation1nstd204human GRCh38.p13 chr19: 36,002,801-36,145,200 , GRCh37.p13 chr19: 36,493,703-36,636,102 LOC101927572, THAP8, 10 more genes
    nsv5281358copy number variation1nstd204human GRCh38.p13 chr19: 36,024,201-36,072,100 , GRCh37.p13 chr19: 36,515,103-36,563,002 CLIP3, RNY5P10, 3 more genes
    nsv5024580copy number variation1nstd200human GRCh38 chr19: 36,024,791-36,025,566 , GRCh37.p13 chr19: 36,515,693-36,516,468 CLIP3, LOC101927572
    nsv5024579copy number variation1nstd200human GRCh38 chr19: 36,005,869-36,025,618 , GRCh37.p13 chr19: 36,496,771-36,516,520 LOC101927572, ALKBH6, 2 more genes
    nsv5024572copy number variation1nstd200human GRCh38 chr19: 35,818,267-36,019,433 , GRCh37.p13 chr19: 36,309,169-36,510,335 SYNE4, LOC107985317, 13 more genes
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4868190copy number variation1nstd200human GRCh37 chr19: 36,515,835-36,516,342 , GRCh38.p12 chr19: 36,024,933-36,025,440 CLIP3, LOC101927572
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4625448copy number variation1nstd183human GRCh37 chr19: 36,505,480-36,505,524 , GRCh38.p12 chr19: 36,014,578-36,014,622 CLIP3, ALKBH6, 1 more genes
    nsv4576808mobile element insertion1nstd166human GRCh37.p13 chr19: 36,518,774-36,518,774 , GRCh38.p12 chr19: 36,027,872-36,027,872 CLIP3, LOC101927572
    nsv4536962copy number variation1nstd166human GRCh37.p13 chr19: 36,309,999-36,510,300 , GRCh38.p12 chr19: 35,819,097-36,019,398 KIRREL2, HCST, 13 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4269221copy number variation1nstd166human GRCh37.p13 chr19: 36,496,850-36,516,478 , GRCh38.p12 chr19: 36,005,948-36,025,576 ALKBH6, LOC101927572, 2 more genes
    nsv4268708copy number variation1nstd166human GRCh37.p13 chr19: 36,522,714-36,523,030 , GRCh38.p12 chr19: 36,031,812-36,032,128 LOC101927572, CLIP3
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