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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5522934copy number variation1nstd206human GRCh38 chr19: 57,711,051-57,854,714 , GRCh37.p13 chr19: 58,222,419-58,366,082 FKBP1AP1, ZNF586, 5 more genes
    nsv5521846copy number variation1nstd206human GRCh38 chr19: 57,774,858-57,779,149 , GRCh37.p13 chr19: 58,286,226-58,290,517 ZNF586
    nsv5520976copy number variation1nstd206human GRCh38 chr19: 57,779,442-57,783,053 , GRCh37.p13 chr19: 58,290,810-58,294,421 ZNF586
    nsv5283991copy number variation1nstd204human GRCh38.p13 chr19: 57,752,101-57,833,900 , GRCh37.p13 chr19: 58,263,469-58,345,268 ZNF586, ZNF587B, 3 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
    nsv5160221mobile element insertion1nstd203human GRCh38 chr19: 57,769,132-57,769,147 , GRCh37.p13 chr19: 58,280,500-58,280,515 ZNF586
    nsv5028209copy number variation1nstd200human GRCh38 chr19: 57,776,693-57,790,408 , GRCh37.p13 chr19: 58,288,061-58,301,776 ZNF586
    nsv5028208copy number variation1nstd200human GRCh38 chr19: 57,767,278-57,770,228 , GRCh37.p13 chr19: 58,278,646-58,281,596 ZNF586
    nsv5025015copy number variation1nstd200human GRCh38 chr19: 57,766,032-57,773,579 , GRCh37.p13 chr19: 58,277,400-58,284,947 ZNF586
    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
    nsv4865381copy number variation1nstd200human GRCh37 chr19: 58,277,386-58,284,951 , GRCh38.p12 chr19: 57,766,018-57,773,583 ZNF586
    nsv4634233copy number variation1nstd183human GRCh37 chr19: 58,284,615-58,345,004 , GRCh38.p12 chr19: 57,773,247-57,833,636 FKBP1AP1, ZNF586, 2 more genes
    nsv4627873copy number variation1nstd183human GRCh37 chr19: 58,264,628-58,388,395 , GRCh38.p12 chr19: 57,753,260-57,877,027 FKBP1AP1, ZNF586, 6 more genes
    nsv4620520copy number variation1nstd183human GRCh37 chr19: 58,290,745-58,294,381 , GRCh38.p12 chr19: 57,779,377-57,783,013 ZNF586
    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
    nsv4457535copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,054,819-58,410,552 , GRCh38.p12 chr19: 57,543,451-57,899,184 ZNF587B, ZNF530, 17 more genes
    nsv4426013copy number variation1nstd174human GRCh37 chr19: 58,271,204-58,390,211 , GRCh38.p12 chr19: 57,759,836-57,878,843 FKBP1AP1, ZNF586, 5 more genes
    nsv4421387copy number variation1nstd174human GRCh37 chr19: 58,281,425-58,298,238 , GRCh38.p12 chr19: 57,770,057-57,786,870 ZNF586
    nsv4381773copy number variation1nstd173human GRCh37 chr19: 58,245,831-58,390,198 , GRCh38.p12 chr19: 57,734,463-57,878,830 FKBP1AP1, ZNF552, 6 more genes
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