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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116369copy number variation1nstd186human GRCh37 chrX: 47,865,198-47,999,028 , GRCh38.p12 chrX: 48,005,800-48,139,600 ZNF630, SSX6P, 3 more genes
    nsv6112721copy number variation1nstd102humanPathogenic GRCh37 chrX: 47,179,068-54,424,785 , GRCh38.p12 chrX: 47,319,669-54,398,352 SNORA11E, SSX11P, 229 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
    nsv5979268copy number variation3nstd209human GRCh38 chrX: 48,107,960-48,127,160 , GRCh37.p13 chrX|NW_004070880.2: 347,389-366,589 , GRCh37.p13 chrX: 47,967,345-47,986,542 SSX6P
    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
    nsv5879433copy number variation1nstd209human GRCh37.p13 chrX: 47,974,914-48,082,075 , GRCh38 chrX: 48,115,532-48,222,640 , GRCh37.p13 chrX|NW_004070880.2: 354,961-462,069 SSX5, SSX6P, 7 more genes
    nsv5876289copy number variation1nstd209human GRCh37.p13 chrX|NW_004070880.2: 256,626-378,769 , GRCh38 chrX: 48,017,197-48,139,340 , GRCh37.p13 chrX: 47,876,592-47,998,761 ZNF630, SSX6P, 2 more genes
    nsv5875851copy number variation1nstd209human GRCh38 chrX: 48,104,938-48,252,190 , GRCh37.p13 chrX|NW_004070880.2: 344,367-491,619 , GRCh37.p13 chrX: 47,964,322-48,111,625 LOC100420083, S100A11P7, 9 more genes
    nsv5669559copy number variation1nstd207human GRCh37.p13 chrX|NW_004070880.2: 355,056-355,182 , GRCh38 chrX: 48,115,627-48,115,753 , GRCh37.p13 chrX: 47,975,009-47,975,135 SSX6P
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5433229copy number variation1nstd206human GRCh38 chrX: 48,109,837-48,127,837 , GRCh37.p13 chrX|NW_004070880.2: 349,266-367,266 , GRCh37.p13 chrX: 47,969,221-47,987,219 SSX6P
    nsv5430513copy number variation1nstd206human GRCh37.p13 chrX|NW_004070880.2: 250,388-372,647 , GRCh38 chrX: 48,010,959-48,133,218 , GRCh37.p13 chrX: 47,870,354-47,992,600 SSX6P, ZNF630-AS1, 2 more genes
    nsv5428316copy number variation2nstd206human GRCh38 chrX: 48,105,837-48,253,837 , GRCh37.p13 chrX|NW_004070880.2: 345,266-493,266 , GRCh37.p13 chrX: 47,965,222-48,113,272 LOC643554, RNU6-707P, 10 more genes
    nsv5427203copy number variation1nstd206human GRCh37.p13 chrX|NW_004070880.2: 245,229-379,029 , GRCh38 chrX: 48,005,800-48,139,600 , GRCh37.p13 chrX: 47,865,198-47,999,028 SSX6P, SPACA5, 3 more genes
    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
    nsv4902692copy number variation1nstd200human GRCh38 chrX: 48,089,218-48,143,196 , GRCh37.p13 chrX|NW_004070880.2: 328,647-382,625 , GRCh37.p13 chrX: 47,948,587-48,002,624 SSX6P, SPACA5B
    nsv4779670copy number variation1nstd200human GRCh37 chrX: 47,977,243-48,022,549 , GRCh38.p12 chrX: 48,117,861-48,163,121 SSX6P, SPACA5B, 3 more genes
    nsv4754671copy number variation1nstd199human GRCh37 chrX: 47,974,867-47,975,074 , GRCh38.p12 chrX: 48,115,485-48,115,692 SSX6P
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