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Items: 1 to 20 of 463

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124242copy number variation1nstd186human GRCh37 chr22: 36,090,982-36,091,252 , GRCh38.p12 chr22|NT_187630.1: 9,702-9,972 , GRCh38.p12 chr22: 35,694,935-35,695,205 0
    nsv6123840copy number variation1nstd186human GRCh37 chr22: 36,090,227-36,096,250 , GRCh38.p12 chr22|NT_187630.1: 8,947-14,970 , GRCh38.p12 chr22: 35,694,180-35,700,203 0
    nsv5392961copy number variation1nstd186human GRCh37 chr22: 36,090,283-36,096,204 , GRCh38.p12 chr22|NT_187630.1: 9,003-14,924 , GRCh38.p12 chr22: 35,694,236-35,700,157 0
    nsv5392850copy number variation1nstd186human GRCh37 chr22: 36,090,281-36,096,204 , GRCh38.p12 chr22|NT_187630.1: 9,001-14,924 , GRCh38.p12 chr22: 35,694,234-35,700,157 0
    nsv5390882copy number variation2nstd186human GRCh37 chr22: 36,133,530-36,134,245 , GRCh38.p12 chr22: 35,737,483-35,738,198 , GRCh38.p12 chr22|NT_187630.1: 58,480-59,195 RBFOX2
    nsv5343748translocation1nstd200human GRCh37 chr22: 36,283,176-36,283,176 , GRCh37 chr22: 36,287,551-36,287,551 , GRCh38.p12 chr22: 35,891,504-35,891,504 , GRCh38.p12 chr22|NT_187630.1: 212,502-212,502 , GRCh38.p12 chr22: 35,887,129-35,887,129 , GRCh38.p12 chr22|NT_187630.1: 208,127-208,127 RBFOX2
    nsv4883640copy number variation1nstd200human GRCh37 chr22: 36,119,475-36,120,261 , GRCh38.p12 chr22: 35,723,428-35,724,214 , GRCh38.p12 chr22|NT_187630.1: 38,196-38,982 APOL5
    nsv4882805copy number variation1nstd200human GRCh37 chr22: 36,228,831-36,231,392 , GRCh38.p12 chr22: 35,832,784-35,835,345 , GRCh38.p12 chr22|NT_187630.1: 153,782-156,343 RBFOX2
    nsv4881972copy number variation1nstd200human GRCh37 chr22: 36,121,656-36,123,781 , GRCh38.p12 chr22|NT_187630.1: 40,376-42,501 , GRCh38.p12 chr22: 35,725,609-35,727,734 APOL5
    nsv4880298copy number variation1nstd200human GRCh37 chr22: 36,090,183-36,096,339 , GRCh38.p12 chr22|NT_187630.1: 8,903-15,059 , GRCh38.p12 chr22: 35,694,136-35,700,292 0
    nsv4878057copy number variation1nstd200human GRCh37 chr22: 36,303,770-36,304,839 , GRCh38.p12 chr22: 35,907,722-35,908,791 , GRCh38.p12 chr22|NT_187630.1: 228,720-229,789 RBFOX2
    nsv4877229copy number variation1nstd200human GRCh37 chr22: 36,315,680-36,336,864 , GRCh38.p12 chr22: 35,919,632-35,940,816 , GRCh38.p12 chr22|NT_187630.1: 240,630-261,814 RBFOX2
    nsv4875998copy number variation1nstd200human GRCh37 chr22: 36,264,074-36,264,582 , GRCh38.p12 chr22: 35,868,027-35,868,535 , GRCh38.p12 chr22|NT_187630.1: 189,025-189,533 RBFOX2
    nsv4874851copy number variation1nstd200human GRCh37 chr22: 36,133,530-36,134,245 , GRCh38.p12 chr22: 35,737,483-35,738,198 , GRCh38.p12 chr22|NT_187630.1: 58,480-59,195 RBFOX2
    nsv4874650copy number variation1nstd200human GRCh37 chr22: 36,195,197-36,195,668 , GRCh38.p12 chr22: 35,799,150-35,799,621 , GRCh38.p12 chr22|NT_187630.1: 120,148-120,619 RBFOX2
    nsv4873764copy number variation1nstd200human GRCh37 chr22: 36,273,059-36,274,423 , GRCh38.p12 chr22: 35,877,012-35,878,376 , GRCh38.p12 chr22|NT_187630.1: 198,010-199,374 RBFOX2
    nsv4872091copy number variation1nstd200human GRCh37 chr22: 36,219,994-36,221,802 , GRCh38.p12 chr22: 35,823,947-35,825,755 , GRCh38.p12 chr22|NT_187630.1: 144,945-146,753 RBFOX2
    nsv4871489copy number variation1nstd200human GRCh37 chr22: 36,221,072-36,221,766 , GRCh38.p12 chr22: 35,825,025-35,825,719 , GRCh38.p12 chr22|NT_187630.1: 146,023-146,717 RBFOX2
    nsv4870342copy number variation1nstd200human GRCh37 chr22: 36,087,879-36,091,694 , GRCh38.p12 chr22: 35,691,832-35,695,647 , GRCh38.p12 chr22|NT_187630.1: 6,599-10,414 0
    nsv4750767insertion1nstd199human GRCh37 chr22: 36,131,347-36,131,347 , GRCh38.p12 chr22: 35,735,300-35,735,300 , GRCh38.p12 chr22|NT_187630.1: 56,303-56,303 0
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