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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131597insertion1nstd186human GRCh37 chr19: 50,894,375-50,894,375 , GRCh38.p12 chr19: 50,391,118-50,391,118 POLD1
    nsv6129324insertion1nstd186human GRCh37 chr19: 50,904,641-50,904,659 , GRCh38.p12 chr19: 50,401,384-50,401,402 POLD1
    nsv6128726copy number variation1nstd186human GRCh37 chr19: 50,907,262-50,907,840 , GRCh38.p12 chr19: 50,404,005-50,404,583 POLD1
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5973445insertion1nstd209human GRCh38 chr19: 50,400,161-50,400,161 , GRCh37.p13 chr19: 50,903,418-50,903,418 POLD1
    nsv5970571inversion1nstd209human GRCh38 chr19: 50,142,503-50,623,829 , GRCh37.p13 chr19: 50,645,760-51,127,086 KCNC3, MYBPC2, 16 more genes
    nsv5968983insertion1nstd209human GRCh38 chr19: 50,391,119-50,391,119 , GRCh37.p13 chr19: 50,894,376-50,894,376 POLD1
    nsv5968950insertion1nstd209human GRCh38 chr19: 50,401,375-50,401,375 , GRCh37.p13 chr19: 50,904,632-50,904,632 POLD1
    nsv5930543copy number variation1nstd209human GRCh38 chr19: 50,395,139-50,395,232 , GRCh37.p13 chr19: 50,898,396-50,898,489 POLD1
    nsv5929216copy number variation1nstd209human GRCh38 chr19: 50,404,297-50,404,612 , GRCh37.p13 chr19: 50,907,554-50,907,869 POLD1
    nsv5649843insertion1nstd207human GRCh38 chr19: 50,391,110-50,391,110 , GRCh37.p13 chr19: 50,894,367-50,894,367 POLD1
    nsv5592424copy number variation1nstd207human GRCh38 chr19: 50,400,134-50,400,210 , GRCh37.p13 chr19: 50,903,391-50,903,467 POLD1
    nsv5588544copy number variation1nstd207human GRCh38 chr19: 50,395,139-50,395,232 , GRCh37.p13 chr19: 50,898,396-50,898,489 POLD1
    nsv5585697copy number variation1nstd207human GRCh38 chr19: 50,404,297-50,404,612 , GRCh37.p13 chr19: 50,907,554-50,907,869 POLD1
    nsv5564403copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,902,099-50,917,146 , GRCh38.p12 chr19: 50,398,842-50,413,889 POLD1
    nsv5564163copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,905,025-50,912,933 , GRCh38.p12 chr19: 50,401,768-50,409,676 POLD1
    nsv5548878insertion1nstd206human GRCh38 chr19: 50,401,384-50,401,402 , GRCh37.p13 chr19: 50,904,641-50,904,659 POLD1
    nsv5535830insertion1nstd206human GRCh38 chr19: 50,391,118-50,391,118 , GRCh37.p13 chr19: 50,894,375-50,894,375 POLD1
    nsv5531586copy number variation1nstd206human GRCh38 chr19: 50,404,005-50,404,583 , GRCh37.p13 chr19: 50,907,262-50,907,840 POLD1
    nsv5522218copy number variation1nstd206human GRCh38 chr19: 50,388,844-50,396,439 , GRCh37.p13 chr19: 50,892,101-50,899,696 POLD1
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