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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920511copy number variation1nstd209human GRCh38 chr9: 96,819,262-96,826,493 , GRCh37.p13 chr9: 99,581,544-99,588,775 ZNF782
    nsv5919577copy number variation1nstd209human GRCh38 chr9: 96,830,373-96,835,103 , GRCh37.p13 chr9: 99,592,655-99,597,385 ZNF782
    nsv5916521copy number variation1nstd209human GRCh38 chr9: 96,831,797-96,835,419 , GRCh37.p13 chr9: 99,594,079-99,597,701 ZNF782
    nsv5859625copy number variation1nstd209human GRCh38 chr9: 96,818,228-96,826,634 , GRCh37.p13 chr9: 99,580,510-99,588,916 ZNF782
    nsv5858884copy number variation1nstd209human GRCh38 chr9: 96,819,328-96,822,627 , GRCh37.p13 chr9: 99,581,610-99,584,909 ZNF782
    nsv5853120copy number variation1nstd209human GRCh38 chr9: 96,830,635-96,836,134 , GRCh37.p13 chr9: 99,592,917-99,598,416 ZNF782
    nsv5713856mobile element insertion2nstd211human GRCh38 chr9: 96,830,842-96,830,842 , GRCh37.p13 chr9: 99,593,124-99,593,124 ZNF782
    nsv5493611copy number variation1nstd206human GRCh38 chr9: 96,815,199-96,815,299 , GRCh37.p13 chr9: 99,577,481-99,577,581 ZNF782
    nsv5489013copy number variation1nstd206human GRCh38 chr9: 96,838,235-96,840,669 , GRCh37.p13 chr9: 99,600,517-99,602,951 ZNF782
    nsv5485310copy number variation1nstd206human GRCh38 chr9: 96,856,726-96,974,338 , GRCh37.p13 chr9: 99,619,008-99,736,620 MFSD14CP, ZNF782, 5 more genes
    nsv5484091copy number variation1nstd206human GRCh38 chr9: 96,822,324-96,822,423 , GRCh37.p13 chr9: 99,584,606-99,584,705 ZNF782
    nsv5396012mobile element insertion1nstd206human GRCh38 chr9: 96,830,842-96,830,893 , GRCh37.p13 chr9: 99,593,124-99,593,175 ZNF782
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5243314copy number variation1nstd204human GRCh38.p13 chr9: 96,838,701-96,842,900 , GRCh37.p13 chr9: 99,600,983-99,605,182 ZNF782
    nsv5127362mobile element insertion1nstd203human GRCh38 chr9: 96,830,774-96,830,788 , GRCh37.p13 chr9: 99,593,056-99,593,070 ZNF782
    nsv5124373mobile element insertion1nstd203human GRCh38 chr9: 96,830,831-96,830,842 , GRCh37.p13 chr9: 99,593,113-99,593,124 ZNF782
    nsv5120617mobile element insertion1nstd203human GRCh38 chr9: 96,830,834-96,830,842 , GRCh37.p13 chr9: 99,593,116-99,593,124 ZNF782
    nsv4982666copy number variation1nstd200human GRCh38 chr9: 96,862,162-96,864,137 , GRCh37.p13 chr9: 99,624,444-99,626,419 ZNF782
    nsv4982665copy number variation1nstd200human GRCh38 chr9: 96,824,115-96,826,939 , GRCh37.p13 chr9: 99,586,397-99,589,221 ZNF782
    nsv4974749copy number variation1nstd200human GRCh38 chr9: 96,819,098-96,823,665 , GRCh37.p13 chr9: 99,581,380-99,585,947 ZNF782
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