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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112722copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,069,104-45,843,277 , GRCh38.p12 chrX: 42,209,851-45,983,842 TATDN2P1, RRM2P3, 36 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
    nsv6112676copy number variation1nstd102humanPathogenic GRCh37 chrX: 44,879,855-46,541,970 , GRCh38.p12 chrX: 45,020,610-46,682,535 KRBOX4, LINC01204, 25 more genes
    nsv5882824copy number variation1nstd209human GRCh38 chrX: 44,722,720-48,672,672 , GRCh37.p13 chrX: 44,581,966-47,619,970 ZNF674-AS1, CDK16, 115 more genes
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5666973copy number variation1nstd207human GRCh38 chrX: 45,155,027-45,155,161 , GRCh37.p13 chrX: 45,014,272-45,014,406 DIPK2B
    nsv5418215copy number variation1nstd206human GRCh38 chrX: 45,157,019-45,158,365 , GRCh37.p13 chrX: 45,016,264-45,017,610 DIPK2B
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905448copy number variation1nstd200human GRCh38 chrX: 44,955,459-45,174,902 , GRCh37.p13 chrX: 44,814,704-45,034,147 DIPK2B, KDM6A
    nsv4771343copy number variation1nstd200human GRCh37 chrX: 45,058,626-45,069,559 , GRCh38.p12 chrX: 45,199,381-45,210,314 DIPK2B
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4673986copy number variation1nstd102humanUncertain significance GRCh37 chrX: 44,931,762-45,166,819 , GRCh38.p12 chrX: 45,072,517-45,307,574 DIPK2B, KDM6A
    nsv4651577copy number variation1nstd186human GRCh37 chrX: 45,016,247-45,017,614 , GRCh38.p12 chrX: 45,157,002-45,158,369 DIPK2B
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4516954copy number variation1nstd166human GRCh37.p13 chrX: 45,013,575-45,014,090 , GRCh38.p12 chrX: 45,154,330-45,154,845 DIPK2B
    nsv4453350copy number variation1nstd102humanUncertain significance GRCh37 chrX: 44,687,226-45,154,972 , GRCh38.p12 chrX: 44,827,980-45,295,727 KDM6A, LOC105373190, 2 more genes
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