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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968517insertion1nstd209human GRCh38 chr14: 80,206,449-80,206,449 , GRCh37.p13 chr14: 80,672,792-80,672,792 DIO2
    nsv5710105mobile element insertion2nstd211human GRCh38 chr14: 80,206,464-80,206,464 , GRCh37.p13 chr14: 80,672,807-80,672,807 DIO2
    nsv5703155mobile element insertion2nstd211human GRCh38 chr14: 80,208,209-80,208,209 , GRCh37.p13 chr14: 80,674,552-80,674,552 DIO2
    nsv5503428copy number variation1nstd206human GRCh38 chr14: 80,197,085-80,340,189 , GRCh37.p13 chr14: 80,663,428-80,806,532 DIO2-AS1, DIO2
    nsv5424983mobile element insertion1nstd206human GRCh38 chr14: 80,208,209-80,208,260 , GRCh37.p13 chr14: 80,674,552-80,674,603 DIO2
    nsv5419269mobile element insertion1nstd206human GRCh38 chr14: 80,206,464-80,206,515 , GRCh37.p13 chr14: 80,672,807-80,672,858 DIO2
    nsv5315062copy number variation1nstd204human GRCh38.p13 chr14: 80,196,927-80,197,234 , GRCh37.p13 chr14: 80,663,270-80,663,577 DIO2
    nsv5306125copy number variation1nstd204human GRCh37.p13 chr14: 80,675,711-80,676,053 , GRCh38.p13 chr14: 80,209,368-80,209,710 DIO2, DIO2-AS1
    nsv5157917mobile element insertion1nstd203human GRCh38 chr14: 80,208,197-80,208,209 , GRCh37.p13 chr14: 80,674,540-80,674,552 DIO2
    nsv5149601mobile element insertion1nstd203human GRCh38 chr14: 80,206,449-80,206,464 , GRCh37.p13 chr14: 80,672,792-80,672,807 DIO2
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004844copy number variation1nstd200human GRCh38 chr14: 80,121,391-80,254,753 , GRCh37.p13 chr14: 80,587,734-80,721,096 LOC105370593, LOC105370591, 2 more genes
    nsv4840140copy number variation1nstd200human GRCh37 chr14: 80,663,274-80,663,574 , GRCh38.p12 chr14: 80,196,931-80,197,231 DIO2
    nsv4626542copy number variation1nstd183human GRCh37 chr14: 80,691,137-80,697,781 , GRCh38.p12 chr14: 80,224,794-80,231,438 DIO2, DIO2-AS1
    nsv4499951mobile element insertion1nstd166human GRCh37.p13 chr14: 80,672,792-80,672,792 , GRCh38.p12 chr14: 80,206,449-80,206,449 DIO2
    nsv4456664copy number variation1nstd102humanPathogenic GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793 DYNLL1P2, GTF2A1, 126 more genes
    nsv4225802copy number variation1nstd166human GRCh37.p13 chr14: 80,663,274-80,663,574 , GRCh38.p12 chr14: 80,196,931-80,197,231 DIO2
    nsv4222498copy number variation1nstd166human GRCh37.p13 chr14: 80,693,083-80,694,628 , GRCh38.p12 chr14: 80,226,740-80,228,285 DIO2-AS1, DIO2
    nsv4218683copy number variation1nstd166human GRCh37.p13 chr14: 80,697,313-80,697,943 , GRCh38.p12 chr14: 80,230,970-80,231,600 DIO2-AS1, DIO2
    nsv3958230insertion1nstd168human GRCh38 chr14: 80,195,121-80,251,496 , GRCh37.p13 chr14: 80,661,464-80,717,839 DIO2, DIO2-AS1
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