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Items: 1 to 20 of 1064

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125268copy number variation1nstd186human GRCh37 chr18: 61,810,786-61,810,843 , GRCh38.p12 chr18: 64,143,552-64,143,609 LINC01924, LINC00305
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    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
    nsv5973144insertion1nstd209human GRCh38 chr18: 64,371,659-64,371,659 , GRCh37.p13 chr18: 62,038,894-62,038,894 LINC01924
    nsv5945859copy number variation1nstd209human GRCh38 chr18: 64,135,469-64,136,238 , GRCh37.p13 chr18: 61,802,703-61,803,472 LINC01924, LINC00305
    nsv5936187copy number variation1nstd209human GRCh38 chr18: 64,374,566-64,375,246 , GRCh37.p13 chr18: 62,041,801-62,042,481 LINC01924
    nsv5929352copy number variation1nstd209human GRCh38 chr18: 64,410,977-64,412,279 , GRCh37.p13 chr18: 62,078,212-62,079,514 LINC01924
    nsv5713354mobile element insertion1nstd211human GRCh38 chr18: 64,300,655-64,300,655 , GRCh37.p13 chr18: 61,967,890-61,967,890 LINC01924
    nsv5713024mobile element insertion2nstd211human GRCh38 chr18: 64,215,570-64,215,570 , GRCh37.p13 chr18: 61,882,805-61,882,805 LINC01924, LINC01538
    nsv5706106mobile element insertion1nstd211human GRCh38 chr18: 64,375,343-64,375,343 , GRCh37.p13 chr18: 62,042,578-62,042,578 LINC01924
    nsv5705690mobile element insertion1nstd211human GRCh38 chr18: 64,357,335-64,357,335 , GRCh37.p13 chr18: 62,024,570-62,024,570 LINC01924
    nsv5704373mobile element insertion1nstd211human GRCh38 chr18: 64,388,027-64,388,027 , GRCh37.p13 chr18: 62,055,262-62,055,262 LINC01924
    nsv5700785mobile element insertion2nstd211human GRCh38 chr18: 64,317,388-64,317,388 , GRCh37.p13 chr18: 61,984,623-61,984,623 LINC01924
    nsv5657438insertion1nstd207human GRCh38 chr18: 64,143,566-64,143,566 , GRCh37.p13 chr18: 61,810,800-61,810,800 LINC01924, LINC00305
    nsv5656214insertion2nstd207human GRCh38 chr18: 64,389,512-64,389,512 , GRCh37.p13 chr18: 62,056,747-62,056,747 LINC01924
    nsv5648451insertion1nstd207human GRCh38 chr18: 64,317,372-64,317,372 , GRCh37.p13 chr18: 61,984,607-61,984,607 LINC01924
    nsv5646365insertion1nstd207human GRCh38 chr18: 64,389,637-64,389,637 , GRCh37.p13 chr18: 62,056,872-62,056,872 LINC01924
    nsv5595040copy number variation1nstd207human GRCh38 chr18: 64,374,566-64,375,246 , GRCh37.p13 chr18: 62,041,801-62,042,481 LINC01924
    nsv5591694copy number variation1nstd207human GRCh38 chr18: 64,318,606-64,318,655 , GRCh37.p13 chr18: 61,985,841-61,985,890 LINC01924
    nsv5586753copy number variation1nstd207human GRCh38 chr18: 64,389,476-64,389,557 , GRCh37.p13 chr18: 62,056,711-62,056,792 LINC01924
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