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Items: 1 to 20 of 250

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945952copy number variation1nstd209human GRCh38 chr17: 78,422,487-78,422,536 , GRCh37.p13 chr17: 76,418,568-76,418,617 PGS1, DNAH17
    nsv5940734copy number variation1nstd209human GRCh38 chr17: 78,385,947-78,386,013 , GRCh37.p13 chr17: 76,382,028-76,382,094 PGS1
    nsv5939241copy number variation1nstd209human GRCh38 chr17: 78,417,066-78,417,201 , GRCh37.p13 chr17: 76,413,147-76,413,282 PGS1
    nsv5931964copy number variation1nstd209human GRCh38 chr17: 78,397,289-78,397,392 , GRCh37.p13 chr17: 76,393,370-76,393,473 PGS1
    nsv5651854insertion1nstd207human GRCh38 chr17: 78,397,289-78,397,289 , GRCh37.p13 chr17: 76,393,370-76,393,370 PGS1
    nsv5648255insertion1nstd207human GRCh38 chr17: 78,422,487-78,422,487 , GRCh37.p13 chr17: 76,418,568-76,418,568 PGS1, DNAH17
    nsv5529343copy number variation1nstd206human GRCh38 chr17: 78,397,054-78,397,116 , GRCh37.p13 chr17: 76,393,135-76,393,197 PGS1
    nsv5527417copy number variation1nstd206human GRCh38 chr17: 78,387,349-78,387,638 , GRCh37.p13 chr17: 76,383,430-76,383,719 PGS1
    nsv5521855copy number variation1nstd206human GRCh38 chr17: 78,397,289-78,397,393 , GRCh37.p13 chr17: 76,393,370-76,393,474 PGS1
    nsv5516393copy number variation1nstd206human GRCh38 chr17: 78,424,410-78,424,508 , GRCh37.p13 chr17: 76,420,491-76,420,589 DNAH17, PGS1
    nsv5515933copy number variation1nstd206human GRCh38 chr17: 78,420,414-78,420,527 , GRCh37.p13 chr17: 76,416,495-76,416,608 PGS1
    nsv5327750copy number variation1nstd204human GRCh38.p13 chr17: 78,397,279-78,397,402 , GRCh37.p13 chr17: 76,393,360-76,393,483 PGS1
    nsv5035778inversion1nstd200human GRCh38 chr17: 78,138,562-78,604,810 , GRCh37.p13 chr17: 76,134,643-76,600,892 , DNAH17-AS1, 20 more genes
    nsv5016889copy number variation1nstd200human GRCh38 chr17: 78,422,916-78,424,729 , GRCh37.p13 chr17: 76,418,997-76,420,810 PGS1, DNAH17
    nsv5016888copy number variation1nstd200human GRCh38 chr17: 78,421,917-78,428,385 , GRCh37.p13 chr17: 76,417,998-76,424,466 PGS1, DNAH17
    nsv5016887copy number variation1nstd200human GRCh38 chr17: 78,407,898-78,408,915 , GRCh37.p13 chr17: 76,403,979-76,404,996 PGS1
    nsv5016886copy number variation1nstd200human GRCh38 chr17: 78,393,256-78,405,164 , GRCh37.p13 chr17: 76,389,337-76,401,245 PGS1
    nsv5016885copy number variation1nstd200human GRCh38 chr17: 78,387,743-78,388,460 , GRCh37.p13 chr17: 76,383,824-76,384,541 PGS1
    nsv5016884copy number variation1nstd200human GRCh38 chr17: 78,385,127-78,387,610 , GRCh37.p13 chr17: 76,381,208-76,383,691 PGS1
    nsv5016883copy number variation1nstd200human GRCh38 chr17: 78,377,258-78,378,256 , GRCh37.p13 chr17: 76,373,339-76,374,337 PGS1
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