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Items: 1 to 20 of 346

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115949mobile element insertion1nstd186human GRCh37 chr18: 23,626,237-23,626,237 , GRCh38.p12 chr18: 26,046,273-26,046,273 SS18
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5969505insertion1nstd209human GRCh38 chr18: 26,046,282-26,046,282 , GRCh37.p13 chr18: 23,626,246-23,626,246 SS18
    nsv5938027copy number variation1nstd209human GRCh38 chr18: 26,041,492-26,050,030 , GRCh37.p13 chr18: 23,621,456-23,629,994 SS18
    nsv5932192copy number variation1nstd209human GRCh38 chr18: 26,053,317-26,053,665 , GRCh37.p13 chr18: 23,633,281-23,633,629 SS18
    nsv5885676copy number variation1nstd209human GRCh38 chr18: 26,041,394-26,050,009 , GRCh37.p13 chr18: 23,621,358-23,629,973 SS18
    nsv5873860copy number variation1nstd209human GRCh38 chr18: 26,043,019-26,044,167 , GRCh37.p13 chr18: 23,622,983-23,624,131 SS18
    nsv5869262copy number variation1nstd209human GRCh38 chr18: 26,046,568-26,047,604 , GRCh37.p13 chr18: 23,626,532-23,627,568 SS18
    nsv5704547mobile element insertion2nstd211human GRCh38 chr18: 26,081,742-26,081,742 , GRCh37.p13 chr18: 23,661,706-23,661,706 SS18
    nsv5702118mobile element insertion1nstd211human GRCh38 chr18: 26,043,945-26,043,945 , GRCh37.p13 chr18: 23,623,909-23,623,909 SS18
    nsv5699307mobile element insertion2nstd211human GRCh38 chr18: 26,046,289-26,046,289 , GRCh37.p13 chr18: 23,626,253-23,626,253 SS18
    nsv5658850insertion1nstd207human GRCh38 chr18: 26,081,730-26,081,730 , GRCh37.p13 chr18: 23,661,694-23,661,694 SS18
    nsv5652527insertion1nstd207human GRCh38 chr18: 26,046,273-26,046,273 , GRCh37.p13 chr18: 23,626,237-23,626,237 SS18
    nsv5585591copy number variation1nstd207human GRCh38 chr18: 26,053,316-26,053,663 , GRCh37.p13 chr18: 23,633,280-23,633,627 SS18
    nsv5547884insertion1nstd206human GRCh38 chr18: 26,081,730-26,081,730 , GRCh37.p13 chr18: 23,661,694-23,661,694 SS18
    nsv5531795copy number variation1nstd206human GRCh38 chr18: 26,041,123-26,045,881 , GRCh37.p13 chr18: 23,621,087-23,625,845 SS18
    nsv5520968copy number variation1nstd206human GRCh38 chr18: 26,053,317-26,053,677 , GRCh37.p13 chr18: 23,633,281-23,633,641 SS18
    nsv5519438copy number variation1nstd206human GRCh38 chr18: 26,046,260-26,046,348 , GRCh37.p13 chr18: 23,626,224-23,626,312 SS18
    nsv5422814mobile element insertion1nstd206human GRCh38 chr18: 26,046,273-26,046,273 , GRCh37.p13 chr18: 23,626,237-23,626,237 SS18
    nsv5349949translocation1nstd200human GRCh38 chr18: 26,053,677-26,053,677 , GRCh38 chr18: 26,053,317-26,053,317 , GRCh37.p13 chr18: 23,633,641-23,633,641 , GRCh37.p13 chr18: 23,633,281-23,633,281 SS18
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