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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979807inversion1nstd209human GRCh38 chr19: 33,158,747-33,171,455 , GRCh37.p13 chr19: 33,649,653-33,662,361 WDR88
    nsv5979328inversion1nstd209human GRCh38 chr19: 32,019,307-33,218,671 , GRCh37.p13 chr19: 32,510,213-33,709,577 , LRP3, 28 more genes
    nsv5936796copy number variation1nstd209human GRCh38 chr19: 33,160,969-33,161,761 , GRCh37.p13 chr19: 33,651,875-33,652,667 WDR88
    nsv5933958copy number variation1nstd209human GRCh38 chr19: 33,136,594-33,136,961 , GRCh37.p13 chr19: 33,627,500-33,627,867 WDR88
    nsv5722047mobile element insertion1nstd211human GRCh38 chr19: 33,134,336-33,134,336 , GRCh37.p13 chr19: 33,625,242-33,625,242 WDR88
    nsv5554846sequence alteration1nstd206human GRCh38 chr19: 33,158,399-33,171,456 , GRCh37.p13 chr19: 33,649,305-33,662,362 WDR88
    nsv5544106insertion1nstd206human GRCh38 chr19: 33,171,454-33,171,454 , GRCh37.p13 chr19: 33,662,360-33,662,360 WDR88
    nsv5532126copy number variation1nstd206human GRCh38 chr19: 33,159,914-33,164,980 , GRCh37.p13 chr19: 33,650,820-33,655,886 WDR88
    nsv5530334copy number variation1nstd206human GRCh38 chr19: 33,150,668-33,150,752 , GRCh37.p13 chr19: 33,641,574-33,641,658 WDR88
    nsv5523287copy number variation1nstd206human GRCh38 chr19: 33,160,531-33,161,748 , GRCh37.p13 chr19: 33,651,437-33,652,654 WDR88
    nsv5523279copy number variation1nstd206human GRCh38 chr19: 33,159,313-33,159,401 , GRCh37.p13 chr19: 33,650,219-33,650,307 WDR88
    nsv5521246copy number variation1nstd206human GRCh38 chr19: 33,158,123-33,158,207 , GRCh37.p13 chr19: 33,649,029-33,649,113 WDR88
    nsv5381195copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,532,300-33,793,320 , GRCh38.p12 chr19: 33,041,394-33,302,414 CEBPA-DT, WDR88, 6 more genes
    nsv5375412translocation1nstd200human GRCh38 chr19: 33,158,751-33,158,751 , GRCh38 chr19: 33,171,456-33,171,456 , GRCh37.p13 chr19: 33,649,657-33,649,657 , GRCh37.p13 chr19: 33,662,362-33,662,362 WDR88
    nsv5337135translocation1nstd200human GRCh37 chr19: 33,649,657-33,649,657 , GRCh37 chr19: 33,662,362-33,662,362 , GRCh38.p12 chr19: 33,171,456-33,171,456 , GRCh38.p12 chr19: 33,158,751-33,158,751 WDR88
    nsv5179397mobile element insertion1nstd203human GRCh38 chr19: 33,136,962-33,137,008 , GRCh37.p13 chr19: 33,627,868-33,627,914 WDR88
    nsv5162149mobile element insertion1nstd203human GRCh38 chr19: 33,162,795-33,162,795 , GRCh37.p13 chr19: 33,653,701-33,653,701 WDR88
    nsv5020366copy number variation1nstd200human GRCh38 chr19: 33,162,823-33,162,899 , GRCh37.p13 chr19: 33,653,729-33,653,805 WDR88
    nsv5020365copy number variation1nstd200human GRCh38 chr19: 33,136,473-33,141,866 , GRCh37.p13 chr19: 33,627,379-33,632,772 WDR88
    nsv5020364copy number variation1nstd200human GRCh38 chr19: 33,136,401-33,137,422 , GRCh37.p13 chr19: 33,627,307-33,628,328 WDR88
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