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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137760copy number variation1nstd102humanBenign GRCh38 chrX: 41,198,367-41,198,431 , GRCh37 chrX: 41,057,620-41,057,684 USP9X
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5885952copy number variation1nstd209human GRCh38 chrX: 41,198,366-41,198,430 , GRCh37.p13 chrX: 41,057,619-41,057,683 USP9X
    nsv5879874copy number variation1nstd209human GRCh38 chrX: 41,098,806-41,099,204 , GRCh37.p13 chrX: 40,958,059-40,958,457 USP9X
    nsv5874893copy number variation1nstd209human GRCh38 chrX: 41,173,875-41,174,850 , GRCh37.p13 chrX: 41,033,128-41,034,103 USP9X
    nsv5873004copy number variation1nstd209human GRCh38 chrX: 37,651,918-42,011,744 , GRCh37.p13 chrX: 37,669,767-41,870,997 , USP9X, 72 more genes
    nsv5715151mobile element insertion1nstd211human GRCh38 chrX: 41,183,834-41,183,834 , GRCh37.p13 chrX: 41,043,087-41,043,087 USP9X
    nsv5671846copy number variation1nstd207human GRCh38 chrX: 41,211,739-41,211,865 , GRCh37.p13 chrX: 41,070,992-41,071,118 USP9X
    nsv5671135copy number variation1nstd207human GRCh38 chrX: 41,198,366-41,198,430 , GRCh37.p13 chrX: 41,057,619-41,057,683 USP9X
    nsv5543403insertion1nstd206human GRCh38 chrX: 41,203,967-41,203,974 , GRCh37.p13 chrX: 41,063,220-41,063,227 USP9X
    nsv5431302copy number variation1nstd206human GRCh38 chrX: 41,198,366-41,198,431 , GRCh37.p13 chrX: 41,057,619-41,057,684 USP9X
    nsv5426592copy number variation1nstd206human GRCh38 chrX: 41,203,947-41,204,018 , GRCh37.p13 chrX: 41,063,200-41,063,271 USP9X
    nsv5423932copy number variation1nstd206human GRCh38 chrX: 41,147,924-41,148,262 , GRCh37.p13 chrX: 41,007,177-41,007,515 USP9X
    nsv5422325copy number variation1nstd206human GRCh38 chrX: 41,124,007-41,124,408 , GRCh37.p13 chrX: 40,983,260-40,983,661 USP9X
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5414133copy number variation1nstd206human GRCh38 chrX: 41,156,718-41,156,954 , GRCh37.p13 chrX: 41,015,971-41,016,207 USP9X
    nsv5381749copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,645,568-44,199,000 , GRCh38.p12 chrX: 39,786,314-44,339,754 EFHC2, GPR82, 58 more genes
    nsv5376130translocation1nstd200human GRCh38 chrX: 41,198,366-41,198,366 , GRCh38 chrX: 41,198,431-41,198,431 , GRCh37.p13 chrX: 41,057,619-41,057,619 , GRCh37.p13 chrX: 41,057,684-41,057,684 USP9X
    nsv5376129translocation1nstd200human GRCh38 chrX: 41,173,877-41,173,877 , GRCh38 chrX: 41,174,851-41,174,851 , GRCh37.p13 chrX: 41,033,130-41,033,130 , GRCh37.p13 chrX: 41,034,104-41,034,104 USP9X
    nsv5376128translocation1nstd200human GRCh38 chrX: 41,098,833-41,098,833 , GRCh38 chrX: 41,099,187-41,099,187 , GRCh37.p13 chrX: 40,958,440-40,958,440 , GRCh37.p13 chrX: 40,958,086-40,958,086 USP9X
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