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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115488copy number variation1nstd186human GRCh37 chrX: 84,509,319-84,509,652 , GRCh38.p12 chrX: 85,254,313-85,254,646 ZNF711
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5966178insertion1nstd209human GRCh38 chrX: 85,254,316-85,254,316 , GRCh37.p13 chrX: 84,509,322-84,509,322 ZNF711
    nsv5872149copy number variation1nstd209human GRCh38 chrX: 85,254,313-85,254,645 , GRCh37.p13 chrX: 84,509,319-84,509,651 ZNF711
    nsv5718687mobile element insertion1nstd211human GRCh38 chrX: 85,248,105-85,248,105 , GRCh37.p13 chrX: 84,503,111-84,503,111 ZNF711
    nsv5666195copy number variation1nstd207human GRCh38 chrX: 85,254,313-85,254,645 , GRCh37.p13 chrX: 84,509,319-84,509,651 ZNF711
    nsv5415743copy number variation1nstd206human GRCh38 chrX: 85,254,313-85,254,646 , GRCh37.p13 chrX: 84,509,319-84,509,652 ZNF711
    nsv5382473copy number variation1nstd186human GRCh37 chrX: 84,509,360-84,509,645 , GRCh38.p12 chrX: 85,254,354-85,254,639 ZNF711
    nsv5195419mobile element insertion1nstd203human GRCh38 chrX: 85,254,568-85,254,646 , GRCh37.p13 chrX: 84,509,574-84,509,652 ZNF711
    nsv5193817mobile element insertion1nstd203human GRCh38 chrX: 85,254,313-85,254,338 , GRCh37.p13 chrX: 84,509,319-84,509,344 ZNF711
    nsv5192686mobile element insertion1nstd203human GRCh38 chrX: 85,254,646-85,254,693 , GRCh37.p13 chrX: 84,509,652-84,509,699 ZNF711
    nsv5189578mobile element insertion1nstd203human GRCh38 chrX: 85,254,638-85,254,646 , GRCh37.p13 chrX: 84,509,644-84,509,652 ZNF711
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4771727copy number variation1nstd200human GRCh37 chrX: 84,509,359-84,509,645 , GRCh38.p12 chrX: 85,254,353-85,254,639 ZNF711
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4766176copy number variation1nstd199human GRCh37 chrX: 84,509,307-84,509,641 , GRCh38.p12 chrX: 85,254,301-85,254,635 ZNF711
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4706308copy number variation3nstd195human GRCh37 chrX: 84,509,319-84,509,320 , GRCh38.p12 chrX: 85,254,313-85,254,314 ZNF711
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