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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940933copy number variation1nstd209human GRCh38 chr19: 57,670,275-57,670,361 , GRCh37.p13 chr19: 58,181,643-58,181,729 ZSCAN4
    nsv5713010mobile element insertion1nstd211human GRCh38 chr19: 57,653,101-57,653,101 , GRCh37.p13 chr19: 58,164,469-58,164,469 ZSCAN4
    nsv5518099copy number variation1nstd206human GRCh38 chr19: 57,650,009-57,650,170 , GRCh37.p13 chr19: 58,161,377-58,161,538 ZSCAN4
    nsv5414376mobile element insertion1nstd206human GRCh38 chr19: 57,653,101-57,653,152 , GRCh37.p13 chr19: 58,164,469-58,164,520 ZSCAN4
    nsv5365866translocation1nstd200human GRCh38 chr19: 57,666,622-57,666,622 , GRCh38 chr19: 57,527,842-57,527,842 , GRCh37.p13 chr19: 58,039,210-58,039,210 , GRCh37.p13 chr19: 58,177,990-58,177,990 ZSCAN4, ZNF549
    nsv5359968translocation1nstd200human GRCh38 chr19: 57,650,382-57,650,382 , GRCh38 chr19: 57,646,597-57,646,597 , GRCh37.p13 chr19: 58,161,750-58,161,750 , GRCh37.p13 chr19: 58,157,965-58,157,965 ZSCAN4
    nsv5334719translocation1nstd200human GRCh37 chr19: 58,177,990-58,177,990 , GRCh37 chr19: 58,039,210-58,039,210 , GRCh38.p12 chr19: 57,527,842-57,527,842 , GRCh38.p12 chr19: 57,666,622-57,666,622 ZSCAN4, ZNF549
    nsv5323662translocation1nstd204human GRCh37.p13 chr19: 58,039,210-58,039,210 , GRCh37.p13 chr19: 58,177,990-58,177,990 , GRCh38.p13 chr19: 57,666,622-57,666,622 , GRCh38.p13 chr19: 57,527,842-57,527,842 ZSCAN4, ZNF549
    nsv5298876copy number variation1nstd204human GRCh38.p13 chr19: 57,666,473-57,721,827 , GRCh37.p13 chr19: 58,177,841-58,233,195 ZSCAN4, ZNF551, 2 more genes
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv5280624copy number variation1nstd204human GRCh38.p13 chr19: 57,527,801-57,913,300 , GRCh37.p13 chr19: 58,039,169-58,424,668 ZNF549, ZNF417, 19 more genes
    nsv5025013copy number variation1nstd200human GRCh38 chr19: 57,662,149-57,967,273 , GRCh37.p13 chr19: 58,173,517-58,478,641 ZNF814, C19orf18, 16 more genes
    nsv4861508copy number variation1nstd200human GRCh37 chr19: 58,161,376-58,161,538 , GRCh38.p12 chr19: 57,650,008-57,650,170 ZSCAN4
    nsv4861507copy number variation1nstd200human GRCh37 chr19: 58,157,960-58,161,750 , GRCh38.p12 chr19: 57,646,592-57,650,382 ZSCAN4
    nsv4631981copy number variation1nstd183human GRCh37 chr19: 58,167,451-58,210,489 , GRCh38.p12 chr19: 57,656,083-57,699,121 ZNF154, ZNF551, 2 more genes
    nsv4575894mobile element insertion1nstd166human GRCh37.p13 chr19: 58,162,366-58,162,366 , GRCh38.p12 chr19: 57,650,998-57,650,998 ZSCAN4
    nsv4512381mobile element insertion1nstd166human GRCh37.p13 chr19: 58,166,678-58,166,678 , GRCh38.p12 chr19: 57,655,310-57,655,310 ZSCAN4
    nsv4506926mobile element insertion1nstd166human GRCh37.p13 chr19: 58,174,710-58,174,710 , GRCh38.p12 chr19: 57,663,342-57,663,342 TPRG1LP1, ZSCAN4
    nsv4457732copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,952,073-58,661,581 , GRCh38.p12 chr19: 57,440,705-58,150,214 ZNF418, ZNF606-AS1, 39 more genes
    nsv4457626copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,092,045-58,686,148 , GRCh38.p12 chr19: 57,580,677-58,174,781 ZNF417, ZSCAN1, 30 more genes
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