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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5972564copy number variation1nstd209human GRCh38 chrX: 66,245,833-66,251,504 , GRCh37.p13 chrX: 65,465,675-65,471,346 HEPH
    nsv5872761copy number variation1nstd209human GRCh38 chrX: 66,246,515-66,248,468 , GRCh37.p13 chrX: 65,466,357-65,468,310 HEPH
    nsv5870253copy number variation1nstd209human GRCh38 chrX: 66,248,675-66,251,428 , GRCh37.p13 chrX: 65,468,517-65,471,270 HEPH
    nsv5715632mobile element insertion1nstd211human GRCh38 chrX: 66,265,851-66,265,851 , GRCh37.p13 chrX: 65,485,693-65,485,693 HEPH
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5433674copy number variation1nstd206human GRCh38 chrX: 66,247,450-66,247,536 , GRCh37.p13 chrX: 65,467,292-65,467,378 HEPH
    nsv5429304copy number variation1nstd206human GRCh38 chrX: 66,165,561-66,165,692 , GRCh37.p13 chrX: 65,385,403-65,385,534 HEPH
    nsv5428790copy number variation1nstd206human GRCh38 chrX: 66,246,475-66,248,511 , GRCh37.p13 chrX: 65,466,317-65,468,353 HEPH
    nsv5418970copy number variation1nstd206human GRCh38 chrX: 66,230,542-66,236,542 , GRCh37.p13 chrX: 65,450,384-65,456,384 HEPH
    nsv5417018copy number variation1nstd206human GRCh38 chrX: 66,246,542-66,252,542 , GRCh37.p13 chrX: 65,466,384-65,472,384 HEPH
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5414776copy number variation1nstd206human GRCh38 chrX: 66,248,635-66,251,471 , GRCh37.p13 chrX: 65,468,477-65,471,313 HEPH
    nsv5376389translocation1nstd200human GRCh38 chrX: 66,248,678-66,248,678 , GRCh38 chrX: 66,251,429-66,251,429 , GRCh37.p13 chrX: 65,471,271-65,471,271 , GRCh37.p13 chrX: 65,468,520-65,468,520 HEPH
    nsv5376388translocation1nstd200human GRCh38 chrX: 66,248,469-66,248,469 , GRCh38 chrX: 66,246,517-66,246,517 , GRCh37.p13 chrX: 65,468,311-65,468,311 , GRCh37.p13 chrX: 65,466,359-65,466,359 HEPH
    nsv5346017translocation1nstd200human GRCh37 chrX: 65,483,294-65,483,294 , GRCh37 chrX: 65,504,143-65,504,143 , GRCh38.p12 chrX: 66,263,452-66,263,452 , GRCh38.p12 chrX: 66,284,301-66,284,301 HEPH
    nsv5334562translocation1nstd200human GRCh37 chrX: 65,478,358-65,478,358 , GRCh37 chrX: 65,502,346-65,502,346 , GRCh38.p12 chrX: 66,282,504-66,282,504 , GRCh38.p12 chrX: 66,258,516-66,258,516 HEPH
    nsv5169501mobile element insertion1nstd203human GRCh38 chrX: 66,265,846-66,265,851 , GRCh37.p13 chrX: 65,485,688-65,485,693 HEPH
    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
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