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Items: 1 to 20 of 494

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977526insertion1nstd209human GRCh38 chr17: 72,484,834-72,484,834 , GRCh37.p13 chr17: 70,480,974-70,480,974 LINC00673
    nsv5934370copy number variation1nstd209human GRCh38 chr17: 72,458,414-72,458,492 , GRCh37.p13 chr17: 70,454,554-70,454,632 LINC00673
    nsv5709278mobile element insertion1nstd211human GRCh38 chr17: 72,564,787-72,564,787 , GRCh37.p13 chr17: 70,560,926-70,560,926 LINC00673
    nsv5698808mobile element insertion2nstd211human GRCh38 chr17: 72,442,201-72,442,201 , GRCh37.p13 chr17: 70,438,341-70,438,341 LINC00673
    nsv5660602insertion1nstd207human GRCh38 chr17: 72,473,469-72,473,469 , GRCh37.p13 chr17: 70,469,609-70,469,609 LINC00673
    nsv5600223copy number variation1nstd207human GRCh38 chr17: 72,473,778-72,473,841 , GRCh37.p13 chr17: 70,469,918-70,469,981 LINC00673
    nsv5598911copy number variation1nstd207human GRCh38 chr17: 72,554,030-72,554,096 , GRCh37.p13 chr17: 70,550,170-70,550,236 LINC00673
    nsv5591010copy number variation1nstd207human GRCh38 chr17: 72,484,787-72,484,836 , GRCh37.p13 chr17: 70,480,927-70,480,976 LINC00673
    nsv5539279insertion1nstd206human GRCh38 chr17: 72,473,412-72,473,412 , GRCh37.p13 chr17: 70,469,552-70,469,552 LINC00673
    nsv5525368copy number variation1nstd206human GRCh38 chr17: 72,565,534-72,570,894 , GRCh37.p13 chr17: 70,561,673-70,567,033 LINC00673
    nsv5524644copy number variation1nstd206human GRCh38 chr17: 72,540,389-72,540,464 , GRCh37.p13 chr17: 70,536,529-70,536,604 LINC00673
    nsv5521527copy number variation1nstd206human GRCh38 chr17: 72,497,668-72,500,780 , GRCh37.p13 chr17: 70,493,808-70,496,920 LINC00673
    nsv5518060copy number variation1nstd206human GRCh38 chr17: 72,541,235-72,543,299 , GRCh37.p13 chr17: 70,537,375-70,539,439 LINC00673
    nsv5517127copy number variation1nstd206human GRCh38 chr17: 72,565,033-72,565,764 , GRCh37.p13 chr17: 70,561,172-70,561,903 LINC00673
    nsv5422627mobile element insertion1nstd206human GRCh38 chr17: 72,442,201-72,442,252 , GRCh37.p13 chr17: 70,438,341-70,438,392 LINC00673
    nsv5375000translocation1nstd200human GRCh38 chr17: 72,565,628-72,565,628 , GRCh38 chr17: 72,570,888-72,570,888 , GRCh37.p13 chr17: 70,561,767-70,561,767 , GRCh37.p13 chr17: 70,567,027-70,567,027 LINC00673
    nsv5349646translocation1nstd200human GRCh38 chr17: 72,452,619-72,452,619 , GRCh38 chr17: 72,452,702-72,452,702 , GRCh37.p13 chr17: 70,448,759-70,448,759 , GRCh37.p13 chr17: 70,448,842-70,448,842 LINC00673
    nsv5349645translocation1nstd200human GRCh38 chr17: 72,446,222-72,446,222 , GRCh38 chr17: 72,445,691-72,445,691 , GRCh37.p13 chr17: 70,441,831-70,441,831 , GRCh37.p13 chr17: 70,442,362-70,442,362 LINC00673
    nsv5333660translocation1nstd200human GRCh37 chr17: 70,442,362-70,442,362 , GRCh37 chr17: 70,441,831-70,441,831 , GRCh38.p12 chr17: 72,445,691-72,445,691 , GRCh38.p12 chr17: 72,446,222-72,446,222 LINC00673
    nsv5329548copy number variation1nstd204human GRCh38.p13 chr17: 72,565,045-72,565,756 , GRCh37.p13 chr17: 70,561,184-70,561,895 LINC00673
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