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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965729insertion1nstd209human GRCh38 chr2: 9,521,840-9,521,840 , GRCh37.p13 chr2: 9,661,969-9,661,969 ADAM17
    nsv5951695insertion1nstd209human GRCh38 chr2: 9,520,937-9,520,937 , GRCh37.p13 chr2: 9,661,066-9,661,066 ADAM17
    nsv5676350mobile element insertion2nstd211human GRCh38 chr2: 9,514,545-9,514,545 , GRCh37.p13 chr2: 9,654,674-9,654,674 , ADAM17
    nsv5611799insertion1nstd207human GRCh38 chr2: 9,520,964-9,520,964 , GRCh37.p13 chr2: 9,661,093-9,661,093 ADAM17
    nsv5536513insertion1nstd206human GRCh38 chr2: 9,521,868-9,521,891 , GRCh37.p13 chr2: 9,661,997-9,662,020 ADAM17
    nsv5448155copy number variation1nstd206human GRCh38 chr2: 9,492,672-9,492,730 , GRCh37.p13 chr2: 9,632,801-9,632,859 ADAM17, IAH1
    nsv5437953copy number variation1nstd206human GRCh38 chr2: 9,502,682-9,503,642 , GRCh37.p13 chr2: 9,642,811-9,643,771 ADAM17, IAH1
    nsv5435175copy number variation1nstd206human GRCh38 chr2: 9,487,480-9,487,550 , GRCh37.p13 chr2: 9,627,609-9,627,679 ADAM17, IAH1
    nsv5299911copy number variation1nstd204human GRCh38.p13 chr2: 9,502,758-9,505,011 , GRCh37.p13 chr2: 9,642,887-9,645,140 IAH1, ADAM17
    nsv5079022mobile element insertion1nstd203human GRCh38 chr2: 9,489,259-9,489,283 , GRCh37.p13 chr2: 9,629,388-9,629,412 ADAM17, IAH1
    nsv5077118mobile element insertion1nstd203human GRCh38 chr2: 9,520,937-9,520,964 , GRCh37.p13 chr2: 9,661,066-9,661,093 ADAM17
    nsv5075088mobile element insertion1nstd203human GRCh38 chr2: 9,536,429-9,536,448 , GRCh37.p13 chr2: 9,676,558-9,676,577 ADAM17
    nsv5067634mobile element insertion1nstd203human GRCh38 chr2: 9,520,936-9,520,964 , GRCh37.p13 chr2: 9,661,065-9,661,093 ADAM17
    nsv4904751copy number variation1nstd200human GRCh38 chr2: 9,503,084-9,504,737 , GRCh37.p13 chr2: 9,643,213-9,644,866 ADAM17, IAH1
    nsv4892286copy number variation1nstd200human GRCh38 chr2: 9,552,149-9,555,113 , GRCh37.p13 chr2: 9,692,278-9,695,242 ADAM17
    nsv4892285copy number variation1nstd200human GRCh38 chr2: 9,523,928-9,524,033 , GRCh37.p13 chr2: 9,664,057-9,664,162 ADAM17
    nsv4892284copy number variation1nstd200human GRCh38 chr2: 9,493,252-9,494,755 , GRCh37.p13 chr2: 9,633,381-9,634,884 ADAM17, IAH1
    nsv4683899copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,630,286-9,695,754 , GRCh38.p12 chr2: 9,490,157-9,555,625 ADAM17, IAH1
    nsv4681081copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,650,088-9,650,280 , GRCh38.p12 chr2: 9,509,959-9,510,151 ADAM17, IAH1
    nsv4584738copy number variation1nstd183human GRCh37 chr2: 9,672,272-9,677,213 , GRCh38.p12 chr2: 9,532,143-9,537,084 ADAM17
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