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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5880859copy number variation1nstd209human GRCh38 chrX: 111,041,204-111,041,427 , GRCh37.p13 chrX: 110,284,432-110,284,655 PAK3
    nsv5880036copy number variation1nstd209human GRCh38 chrX: 111,096,307-111,096,369 , GRCh37.p13 chrX: 110,339,535-110,339,597 PAK3
    nsv5871305copy number variation1nstd209human GRCh38 chrX: 111,171,390-111,171,449 , GRCh37.p13 chrX: 110,414,618-110,414,677 PAK3
    nsv5729132mobile element insertion1nstd211human GRCh38 chrX: 111,058,485-111,058,485 , GRCh37.p13 chrX: 110,301,713-110,301,713 PAK3
    nsv5728174mobile element insertion1nstd211human GRCh38 chrX: 111,091,919-111,091,919 , GRCh37.p13 chrX: 110,335,147-110,335,147 PAK3
    nsv5725098mobile element insertion2nstd211human GRCh38 chrX: 111,029,851-111,029,851 , GRCh37.p13 chrX: 110,273,079-110,273,079 PAK3
    nsv5722398mobile element insertion1nstd211human GRCh38 chrX: 111,089,358-111,089,358 , GRCh37.p13 chrX: 110,332,586-110,332,586 PAK3
    nsv5613175insertion1nstd207human GRCh38 chrX: 111,093,753-111,093,753 , GRCh37.p13 chrX: 110,336,981-110,336,981 PAK3
    nsv5605176insertion1nstd207human GRCh38 chrX: 111,095,417-111,095,417 , GRCh37.p13 chrX: 110,338,645-110,338,645 PAK3
    nsv5563656mobile element insertion1nstd206human GRCh38 chrX: 111,029,851-111,029,902 , GRCh37.p13 chrX: 110,273,079-110,273,130 PAK3
    nsv5558137mobile element insertion1nstd206human GRCh38 chrX: 111,091,919-111,091,970 , GRCh37.p13 chrX: 110,335,147-110,335,198 PAK3
    nsv5536086insertion1nstd206human GRCh38 chrX: 111,028,039-111,028,078 , GRCh37.p13 chrX: 110,271,267-110,271,306 PAK3
    nsv5430932copy number variation1nstd206human GRCh38 chrX: 111,222,116-111,222,166 , GRCh37.p13 chrX: 110,465,344-110,465,394 PAK3
    nsv5429363copy number variation1nstd206human GRCh38 chrX: 111,171,390-111,171,450 , GRCh37.p13 chrX: 110,414,618-110,414,678 PAK3
    nsv5415047copy number variation1nstd206human GRCh38 chrX: 111,193,361-111,193,540 , GRCh37.p13 chrX: 110,436,589-110,436,768 PAK3
    nsv5376877translocation1nstd200human GRCh38 chrX: 111,160,412-111,160,412 , GRCh38 chrX: 111,162,273-111,162,273 , GRCh37.p13 chrX: 110,405,501-110,405,501 , GRCh37.p13 chrX: 110,403,640-110,403,640 PAK3
    nsv5376876translocation1nstd200human GRCh38 chrX: 111,116,452-111,116,452 , GRCh38 chrX: 111,122,360-111,122,360 , GRCh37.p13 chrX: 110,359,680-110,359,680 , GRCh37.p13 chrX: 110,365,588-110,365,588 PAK3
    nsv5376875translocation1nstd200human GRCh38 chrX: 111,122,016-111,122,016 , GRCh38 chrX: 111,097,629-111,097,629 , GRCh37.p13 chrX: 110,340,857-110,340,857 , GRCh37.p13 chrX: 110,365,244-110,365,244 PAK3
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