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Items: 1 to 20 of 952

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968604inversion1nstd209human GRCh38 chr2: 49,436,021-59,087,697 , GRCh37.p13 chr2: 49,663,159-59,314,832 , ACYP2, 95 more genes
    nsv5959046insertion1nstd209human GRCh38 chr2: 58,851,644-58,851,644 , GRCh37.p13 chr2: 59,078,779-59,078,779 LINC01122
    nsv5951992insertion1nstd209human GRCh38 chr2: 58,986,622-58,986,622 , GRCh37.p13 chr2: 59,213,757-59,213,757 LINC01122
    nsv5887280copy number variation1nstd209human GRCh38 chr2: 58,868,972-58,869,608 , GRCh37.p13 chr2: 59,096,107-59,096,743 LINC01122
    nsv5886061copy number variation1nstd209human GRCh38 chr2: 58,768,317-58,769,232 , GRCh37.p13 chr2: 58,995,452-58,996,367 LINC01122
    nsv5882497copy number variation1nstd209human GRCh38 chr2: 58,996,487-58,998,679 , GRCh37.p13 chr2: 59,223,622-59,225,814 LINC01122
    nsv5881184copy number variation1nstd209human GRCh38 chr2: 58,700,271-58,700,403 , GRCh37.p13 chr2: 58,927,406-58,927,538 LINC01122
    nsv5880818copy number variation1nstd209human GRCh38 chr2: 59,045,633-59,046,043 , GRCh37.p13 chr2: 59,272,768-59,273,178 LINC01122
    nsv5880655copy number variation1nstd209human GRCh38 chr2: 58,773,799-58,775,013 , GRCh37.p13 chr2: 59,000,934-59,002,148 LINC01122
    nsv5877451copy number variation1nstd209human GRCh38 chr2: 58,685,659-58,685,711 , GRCh37.p13 chr2: 58,912,794-58,912,846 LINC01122
    nsv5875181copy number variation1nstd209human GRCh38 chr2: 58,542,349-58,542,406 , GRCh37.p13 chr2: 58,769,484-58,769,541 LINC01122
    nsv5871454copy number variation1nstd209human GRCh38 chr2: 58,559,979-58,560,061 , GRCh37.p13 chr2: 58,787,114-58,787,196 LINC01122
    nsv5871053copy number variation1nstd209human GRCh38 chr2: 58,680,314-58,690,692 , GRCh37.p13 chr2: 58,907,449-58,917,827 LINC01122
    nsv5867987copy number variation1nstd209human GRCh38 chr2: 58,726,372-58,730,647 , GRCh37.p13 chr2: 58,953,507-58,957,782 LINC01122
    nsv5833664copy number variation1nstd209human GRCh38 chr2: 58,726,308-58,730,709 , GRCh37.p13 chr2: 58,953,443-58,957,844 LINC01122
    nsv5833337copy number variation1nstd209human GRCh38 chr2: 58,680,337-58,690,560 , GRCh37.p13 chr2: 58,907,472-58,917,695 LINC01122
    nsv5726434mobile element insertion1nstd211human GRCh38 chr2: 59,028,704-59,028,704 , GRCh37.p13 chr2: 59,255,839-59,255,839 LINC01122
    nsv5720993mobile element insertion2nstd211human GRCh38 chr2: 58,909,807-58,909,807 , GRCh37.p13 chr2: 59,136,942-59,136,942 LINC01122
    nsv5720431mobile element insertion1nstd211human GRCh38 chr2: 58,603,369-58,603,369 , GRCh37.p13 chr2: 58,830,504-58,830,504 LINC01122
    nsv5716851mobile element insertion1nstd211human GRCh38 chr2: 58,727,712-58,727,712 , GRCh37.p13 chr2: 58,954,847-58,954,847 LINC01122
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