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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934046copy number variation1nstd209human GRCh38 chr15: 90,350,832-90,352,923 , GRCh37.p13 chr15: 90,894,064-90,896,155 ZNF774
    nsv5933147copy number variation1nstd209human GRCh38 chr15: 90,354,115-90,354,164 , GRCh37.p13 chr15: 90,897,347-90,897,396 ZNF774
    nsv5877258copy number variation1nstd209human GRCh38 chr15: 90,351,013-90,352,913 , GRCh37.p13 chr15: 90,894,245-90,896,145 ZNF774
    nsv5728924mobile element insertion2nstd211human GRCh38 chr15: 90,357,030-90,357,030 , GRCh37.p13 chr15: 90,900,262-90,900,262 ZNF774
    nsv5562365mobile element insertion1nstd206human GRCh38 chr15: 90,357,030-90,357,081 , GRCh37.p13 chr15: 90,900,262-90,900,313 ZNF774
    nsv5531658copy number variation1nstd206human GRCh38 chr15: 90,350,828-90,352,924 , GRCh37.p13 chr15: 90,894,060-90,896,156 ZNF774
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5319830copy number variation1nstd204human GRCh38.p13 chr15: 90,350,961-90,372,856 , GRCh37.p13 chr15: 90,894,193-90,916,088 ZNF774
    nsv5278323copy number variation1nstd204human GRCh38.p13 chr15: 90,350,889-90,372,921 , GRCh37.p13 chr15: 90,894,121-90,916,153 ZNF774
    nsv5265339copy number variation1nstd204human GRCh38.p13 chr15: 90,350,901-90,372,800 , GRCh37.p13 chr15: 90,894,133-90,916,032 ZNF774
    nsv5193903mobile element insertion1nstd203human GRCh38 chr15: 90,357,016-90,357,030 , GRCh37.p13 chr15: 90,900,248-90,900,262 ZNF774
    nsv5009173copy number variation1nstd200human GRCh38 chr15: 90,351,137-90,356,001 , GRCh37.p13 chr15: 90,894,369-90,899,233 ZNF774
    nsv5009170copy number variation1nstd200human GRCh38 chr15: 90,301,150-90,410,414 , GRCh37.p13 chr15: 90,844,382-90,953,646 ZNF774, GOLGA2P8, 3 more genes
    nsv5009168copy number variation1nstd200human GRCh38 chr15: 90,236,762-90,472,930 , GRCh37.p13 chr15: 90,779,994-91,016,162 ZNF774, GDPGP1, 9 more genes
    nsv5002344copy number variation1nstd200human GRCh38 chr15: 90,350,969-90,372,849 , GRCh37.p13 chr15: 90,894,201-90,916,081 ZNF774
    nsv5002343copy number variation1nstd200human GRCh38 chr15: 90,350,830-90,352,924 , GRCh37.p13 chr15: 90,894,062-90,896,156 ZNF774
    nsv4856312copy number variation1nstd200human GRCh37 chr15: 90,894,201-90,916,081 , GRCh38.p12 chr15: 90,350,969-90,372,849 ZNF774
    nsv4856311copy number variation1nstd200human GRCh37 chr15: 90,894,061-90,896,156 , GRCh38.p12 chr15: 90,350,829-90,352,924 ZNF774
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4723623mobile element insertion1nstd186human GRCh37 chr15: 90,900,248-90,900,248 , GRCh38.p12 chr15: 90,357,016-90,357,016 ZNF774
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