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Items: 1 to 20 of 474

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5977834copy number variation1nstd209human GRCh38 chrX: 72,571,948-72,589,683 , GRCh37.p13 chrX|NW_004070882.1: 260,965-278,700 , GRCh37.p13 chrX: 71,791,798-71,809,533 HDAC8, PHKA1
    nsv5974789copy number variation1nstd209human GRCh38 chrX: 72,378,016-72,383,215 , GRCh37.p13 chrX|NW_004070882.1: 67,033-72,232 , GRCh37.p13 chrX: 71,597,866-71,603,065 HDAC8
    nsv5970825copy number variation1nstd209human GRCh38 chrX: 72,383,616-72,388,115 , GRCh37.p13 chrX|NW_004070882.1: 72,633-77,132 , GRCh37.p13 chrX: 71,603,466-71,607,965 HDAC8
    nsv5969694inversion1nstd209human GRCh38 chrX: 72,380,835-72,384,439 , GRCh37.p13 chrX|NW_004070882.1: 69,852-73,456 , GRCh37.p13 chrX: 71,600,685-71,604,289 HDAC8
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5880282copy number variation1nstd209human GRCh38 chrX: 72,426,665-72,426,764 , GRCh37.p13 chrX|NW_004070882.1: 115,682-115,781 , GRCh37.p13 chrX: 71,646,515-71,646,614 HDAC8
    nsv5722637mobile element insertion1nstd211human GRCh38 chrX: 72,541,186-72,541,186 , GRCh37.p13 chrX|NW_004070882.1: 230,203-230,203 , GRCh37.p13 chrX: 71,761,036-71,761,036 HDAC8
    nsv5721430mobile element insertion1nstd211human GRCh38 chrX: 72,503,115-72,503,115 , GRCh37.p13 chrX: 71,722,965-71,722,965 , GRCh37.p13 chrX|NW_004070882.1: 192,132-192,132 HDAC8
    nsv5720359mobile element insertion1nstd211human GRCh38 chrX: 72,562,320-72,562,320 , GRCh37.p13 chrX|NW_004070882.1: 251,337-251,337 , GRCh37.p13 chrX: 71,782,170-71,782,170 HDAC8
    nsv5718513mobile element insertion2nstd211human GRCh38 chrX: 72,531,747-72,531,747 , GRCh37.p13 chrX|NW_004070882.1: 220,764-220,764 , GRCh37.p13 chrX: 71,751,597-71,751,597 HDAC8
    nsv5716940mobile element insertion1nstd211human GRCh38 chrX: 72,429,036-72,429,036 , GRCh37.p13 chrX|NW_004070882.1: 118,053-118,053 , GRCh37.p13 chrX: 71,648,886-71,648,886 HDAC8
    nsv5609642insertion1nstd207human GRCh38 chrX: 72,453,487-72,453,487 , GRCh37.p13 chrX: 71,673,337-71,673,337 , GRCh37.p13 chrX|NW_004070882.1: 142,504-142,504 HDAC8
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5557309mobile element insertion1nstd206human GRCh38 chrX: 72,531,747-72,531,798 , GRCh37.p13 chrX|NW_004070882.1: 220,764-220,815 , GRCh37.p13 chrX: 71,751,597-71,751,648 HDAC8
    nsv5556257mobile element insertion1nstd206human GRCh38 chrX: 72,503,115-72,503,166 , GRCh37.p13 chrX|NW_004070882.1: 192,132-192,183 , GRCh37.p13 chrX: 71,722,965-71,723,016 HDAC8
    nsv5554466mobile element insertion1nstd206human GRCh38 chrX: 72,541,186-72,541,237 , GRCh37.p13 chrX|NW_004070882.1: 230,203-230,254 , GRCh37.p13 chrX: 71,761,036-71,761,087 HDAC8
    nsv5430447copy number variation1nstd206human GRCh38 chrX: 71,740,771-72,518,210 , GRCh37.p13 chrX: 70,960,621-71,530,833 LOC101060274, CXorf49B, 15 more genes
    nsv5430025copy number variation1nstd206human GRCh38 chrX: 72,426,666-72,426,765 , GRCh37.p13 chrX|NW_004070882.1: 115,683-115,782 , GRCh37.p13 chrX: 71,646,516-71,646,615 HDAC8
    nsv5426996copy number variation1nstd206human GRCh38 chrX: 72,537,466-72,537,945 , GRCh37.p13 chrX: 71,757,316-71,757,795 , GRCh37.p13 chrX|NW_004070882.1: 226,483-226,962 HDAC8
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