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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5646653insertion1nstd207human GRCh38 chr19: 44,709,467-44,709,467 , GRCh37.p13 chr19: 45,212,739-45,212,739 CEACAM16, CEACAM16-AS1
    nsv5542570insertion1nstd206human GRCh38 chr19: 44,702,121-44,702,156 , GRCh37.p13 chr19: 45,205,391-45,205,426 CEACAM16, CEACAM16-AS1
    nsv5391340copy number variation1nstd186human GRCh37 chr19: 45,212,381-45,213,200 , GRCh38.p12 chr19: 44,709,109-44,709,928 CEACAM16, CEACAM16-AS1
    nsv5174921mobile element insertion1nstd203human GRCh38 chr19: 44,702,105-44,702,121 , GRCh37.p13 chr19: 45,205,375-45,205,391 CEACAM16-AS1, CEACAM16
    nsv5020642copy number variation1nstd200human GRCh38 chr19: 44,697,442-44,705,349 , GRCh37.p13 chr19: 45,200,712-45,208,619 CEACAM16-AS1, CEACAM16
    nsv5020641copy number variation1nstd200human GRCh38 chr19: 44,697,484-44,698,564 , GRCh37.p13 chr19: 45,200,754-45,201,834 CEACAM16, CEACAM16-AS1
    nsv5020640copy number variation1nstd200human GRCh38 chr19: 44,693,346-44,712,016 , GRCh37.p13 chr19: 45,196,616-45,215,287 CEACAM16-AS1, CEACAM16
    nsv4865201copy number variation1nstd200human GRCh37 chr19: 45,212,381-45,213,200 , GRCh38.p12 chr19: 44,709,109-44,709,928 CEACAM16, CEACAM16-AS1
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4629718copy number variation1nstd183human GRCh37 chr19: 45,202,052-45,329,786 , GRCh38.p12 chr19: 44,698,782-44,826,529 BCL3, BCAM, 4 more genes
    nsv4625911copy number variation1nstd183human GRCh37 chr19: 45,176,041-45,287,600 , GRCh38.p12 chr19: 44,672,769-44,784,343 BCL3, CBLC, 5 more genes
    nsv4623840copy number variation1nstd183human GRCh37 chr19: 45,020,272-45,216,013 , GRCh38.p12 chr19: 44,516,211-44,712,744 PVR, CEACAM19, 7 more genes
    nsv4536199copy number variation1nstd166human GRCh37.p13 chr19: 45,212,374-45,213,158 , GRCh38.p12 chr19: 44,709,102-44,709,886 CEACAM16, CEACAM16-AS1
    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
    nsv4436634complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 43,997,366-44,819,487 , GRCh37 chr19: 44,501,518-45,322,744 BCL3, BCAM, 34 more genes
    nsv4262510copy number variation1nstd166human GRCh37.p13 chr19: 45,198,900-45,204,000 , GRCh38.p12 chr19: 44,695,630-44,700,730 CEACAM16, CEACAM16-AS1
    nsv4257208copy number variation1nstd166human GRCh37.p13 chr19: 45,198,627-45,203,515 , GRCh38.p12 chr19: 44,695,357-44,700,245 CEACAM16, CEACAM16-AS1
    nsv4256858copy number variation1nstd166human GRCh37.p13 chr19: 45,212,356-45,212,415 , GRCh38.p12 chr19: 44,709,084-44,709,143 CEACAM16-AS1, CEACAM16
    nsv3963428insertion1nstd168human GRCh38 chr19: 44,695,767-44,710,536 , GRCh37.p13 chr19: 45,199,037-45,213,808 CEACAM16, CEACAM16-AS1
    nsv3957016copy number variation1nstd168human GRCh38 chr19: 44,663,384-44,726,466 , GRCh37.p13 chr19: 45,166,651-45,229,729 PVR, CEACAM16-AS1, 3 more genes
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