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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5717778mobile element insertion1nstd211human GRCh38 chr10: 124,947,378-124,947,378 , GRCh37.p13 chr10: 126,635,947-126,635,947 ZRANB1
    nsv5561402mobile element insertion1nstd206human GRCh38 chr10: 124,947,392-124,947,429 , GRCh37.p13 chr10: 126,635,961-126,635,998 ZRANB1
    nsv5507680copy number variation1nstd206human GRCh38 chr10: 124,954,591-124,955,339 , GRCh37.p13 chr10: 126,643,160-126,643,908 ZRANB1
    nsv5494090copy number variation1nstd206human GRCh38 chr10: 124,987,934-124,988,002 , GRCh37.p13 chr10: 126,676,503-126,676,571 CTBP2, ZRANB1
    nsv5354563translocation1nstd200human GRCh38 chr10: 124,987,934-124,987,934 , GRCh38 chr10: 124,988,002-124,988,002 , GRCh37.p13 chr10: 126,676,571-126,676,571 , GRCh37.p13 chr10: 126,676,503-126,676,503 ZRANB1, CTBP2
    nsv5315932copy number variation1nstd204human GRCh38.p13 chr10: 124,932,341-124,937,603 , GRCh37.p13 chr10: 126,620,910-126,626,172 ZRANB1
    nsv5129678mobile element insertion1nstd203human GRCh38 chr10: 124,944,957-124,944,973 , GRCh37.p13 chr10: 126,633,526-126,633,542 ZRANB1
    nsv5035234inversion1nstd200human GRCh38 chr10: 124,977,666-124,978,768 , GRCh37.p13 chr10: 126,666,235-126,667,337 ZRANB1
    nsv4977400copy number variation1nstd200human GRCh38 chr10: 124,952,874-124,954,653 , GRCh37.p13 chr10: 126,641,443-126,643,222 ZRANB1
    nsv4841456copy number variation1nstd200human GRCh37 chr10: 126,641,443-126,643,222 , GRCh38.p12 chr10: 124,952,874-124,954,653 ZRANB1
    nsv4711720copy number variation2nstd195human GRCh37 chr10: 126,676,901-126,678,251 , GRCh38.p12 chr10: 124,988,332-124,989,682 CTBP2, ZRANB1
    nsv4711293copy number variation1nstd195human GRCh37 chr10: 126,676,951-126,678,151 , GRCh38.p12 chr10: 124,988,382-124,989,582 CTBP2, ZRANB1
    nsv4710299copy number variation1nstd195human GRCh37 chr10: 126,676,951-126,677,501 , GRCh38.p12 chr10: 124,988,382-124,988,932 CTBP2, ZRANB1
    nsv4702009translocation1nstd195human GRCh38.p12 chrY: 56,856,622-56,856,622 , GRCh37 chrY: 59,002,769-59,002,769 , GRCh38.p12 chr10: 124,988,375-124,988,375 , GRCh37 chr10: 126,676,944-126,676,944 , GRCh38.p12 chrY|NW_009646209.1: 69,870-69,870 CTBP2, ZRANB1, 1 more genes
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4487147mobile element insertion1nstd166human GRCh37.p13 chr10: 126,648,376-126,648,376 , GRCh38.p12 chr10: 124,959,807-124,959,807 ZRANB1
    nsv4482076mobile element insertion1nstd166human GRCh37.p13 chr10: 126,633,526-126,633,526 , GRCh38.p12 chr10: 124,944,957-124,944,957 ZRANB1
    nsv4456733copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,988,334-135,427,143 , GRCh38.p12 chr10: 123,228,818-133,613,639 FAM53B-AS1, LOC105378544, 153 more genes
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