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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965453insertion1nstd209human GRCh38 chr6: 165,943,346-165,943,346 , GRCh37.p13 chr6: 166,356,834-166,356,834 LINC00473, PDE10A
    nsv5956709insertion1nstd209human GRCh38 chr6: 165,958,567-165,958,567 , GRCh37.p13 chr6: 166,372,055-166,372,055 PDE10A, LINC00473
    nsv5916298copy number variation1nstd209human GRCh38 chr6: 165,960,842-165,977,963 , GRCh37.p13 chr6: 166,374,330-166,391,451 LINC00473, PDE10A
    nsv5908797copy number variation1nstd209human GRCh38 chr6: 165,982,908-165,983,175 , GRCh37.p13 chr6: 166,396,396-166,396,663 LINC00473, PDE10A
    nsv5844191copy number variation1nstd209human GRCh38 chr6: 165,962,759-165,977,965 , GRCh37.p13 chr6: 166,376,247-166,391,453 PDE10A, LINC00473
    nsv5688590mobile element insertion1nstd211human GRCh38 chr6: 165,963,139-165,963,139 , GRCh37.p13 chr6: 166,376,627-166,376,627 PDE10A, LINC00473
    nsv5635324insertion1nstd207human GRCh38 chr6: 165,958,539-165,958,539 , GRCh37.p13 chr6: 166,372,027-166,372,027 LINC00473, PDE10A
    nsv5583113copy number variation1nstd207human GRCh38 chr6: 165,929,998-165,930,057 , GRCh37.p13 chr6: 166,343,486-166,343,545 PDE10A, LINC00473
    nsv5395239mobile element insertion1nstd206human GRCh38 chr6: 165,963,139-165,963,190 , GRCh37.p13 chr6: 166,376,627-166,376,678 PDE10A, LINC00473
    nsv4968655copy number variation1nstd200human GRCh38 chr6: 165,587,706-166,398,601 , GRCh37.p13 chr6: 166,001,194-166,812,089 LOC105378115, TBXT, 19 more genes
    nsv4965918copy number variation1nstd200human GRCh38 chr6: 165,982,474-165,988,982 , GRCh37.p13 chr6: 166,395,962-166,402,470 PDE10A, LINC00473, 1 more genes
    nsv4965917copy number variation1nstd200human GRCh38 chr6: 165,964,647-165,965,847 , GRCh37.p13 chr6: 166,378,135-166,379,335 PDE10A, LINC00473
    nsv4965916copy number variation1nstd200human GRCh38 chr6: 165,958,022-165,958,850 , GRCh37.p13 chr6: 166,371,510-166,372,338 LINC00473, PDE10A
    nsv4965915copy number variation1nstd200human GRCh38 chr6: 165,956,186-165,956,314 , GRCh37.p13 chr6: 166,369,674-166,369,802 PDE10A, LINC00473
    nsv4965914copy number variation1nstd200human GRCh38 chr6: 165,940,700-165,942,792 , GRCh37.p13 chr6: 166,354,188-166,356,280 LINC00473, PDE10A
    nsv4824887copy number variation1nstd200human GRCh37 chr6: 166,001,194-166,812,089 , GRCh38.p12 chr6: 165,587,706-166,398,601 GNG5P1, LOC107986668, 19 more genes
    nsv4818028copy number variation1nstd200human GRCh37 chr6: 166,339,708-166,353,796 , GRCh38.p12 chr6: 165,926,220-165,940,308 LINC00473, PDE10A
    nsv4763261insertion1nstd199human GRCh37 chr6: 166,371,958-166,371,958 , GRCh38.p12 chr6: 165,958,470-165,958,470 PDE10A, LINC00473
    nsv4730863copy number variation1nstd199human GRCh37 chr6: 166,343,520-166,343,580 , GRCh38.p12 chr6: 165,930,032-165,930,092 PDE10A, LINC00473
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
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