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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5977805copy number variation1nstd209human GRCh38 chrX: 54,237,230-54,247,164 , GRCh37.p13 chrX|NW_004070877.1: 3,950,345-3,960,279 , GRCh37.p13 chrX: 54,263,663-54,273,597 WNK3
    nsv5949922insertion1nstd209human GRCh38 chrX: 54,213,564-54,213,564 , GRCh37.p13 chrX|NW_004070877.1: 3,926,679-3,926,679 , GRCh37.p13 chrX: 54,239,997-54,239,997 WNK3
    nsv5882057copy number variation1nstd209human GRCh38 chrX: 52,862,950-55,652,570 , GRCh37.p13 chrX: 52,891,979-54,424,077 , GRCh37.p13 chrX|NW_004070877.1: 2,576,065-4,110,759 , MIRLET7F2, 64 more genes
    nsv5871458copy number variation1nstd209human GRCh38 chrX: 54,192,446-54,192,497 , GRCh37.p13 chrX: 54,218,879-54,218,930 , GRCh37.p13 chrX|NW_004070877.1: 3,905,561-3,905,612 WNK3
    nsv5720698mobile element insertion2nstd211human GRCh38 chrX: 54,327,517-54,327,517 , GRCh37.p13 chrX: 54,353,950-54,353,950 , GRCh37.p13 chrX|NW_004070877.1: 4,040,632-4,040,632 WNK3
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5432837copy number variation1nstd206human GRCh38 chrX: 54,284,407-54,284,611 , GRCh37.p13 chrX: 54,310,840-54,311,044 , GRCh37.p13 chrX|NW_004070877.1: 3,997,522-3,997,726 WNK3
    nsv5429503copy number variation1nstd206human GRCh38 chrX: 54,319,738-54,320,570 , GRCh37.p13 chrX: 54,346,171-54,347,003 , GRCh37.p13 chrX|NW_004070877.1: 4,032,853-4,033,685 WNK3
    nsv5428851copy number variation1nstd206human GRCh38 chrX: 54,318,277-54,318,602 , GRCh37.p13 chrX: 54,344,710-54,345,035 , GRCh37.p13 chrX|NW_004070877.1: 4,031,392-4,031,717 WNK3
    nsv5425998copy number variation1nstd206human GRCh38 chrX: 54,225,734-54,225,798 , GRCh37.p13 chrX|NW_004070877.1: 3,938,849-3,938,913 , GRCh37.p13 chrX: 54,252,167-54,252,231 WNK3
    nsv5417231copy number variation1nstd206human GRCh38 chrX: 54,358,822-54,358,979 , GRCh37.p13 chrX: 54,385,255-54,385,412 , GRCh37.p13 chrX|NW_004070877.1: 4,071,937-4,072,094 WNK3
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5416410copy number variation1nstd206human GRCh38 chrX: 54,218,652-54,219,488 , GRCh37.p13 chrX: 54,245,085-54,245,921 , GRCh37.p13 chrX|NW_004070877.1: 3,931,767-3,932,603 WNK3
    nsv5416005copy number variation1nstd206human GRCh38 chrX: 54,225,369-54,226,618 , GRCh37.p13 chrX|NW_004070877.1: 3,938,484-3,939,733 , GRCh37.p13 chrX: 54,251,802-54,253,051 WNK3
    nsv5376239translocation1nstd200human GRCh38 chrX: 54,331,203-54,331,203 , GRCh38 chrX: 54,331,265-54,331,265 , GRCh37.p13 chrX|NW_004070877.1: 4,044,318-4,044,318 , GRCh37.p13 chrX|NW_004070877.1: 4,044,380-4,044,380 , GRCh37.p13 chrX: 54,357,636-54,357,636 , GRCh37.p13 chrX: 54,357,698-54,357,698 WNK3
    nsv5376238translocation1nstd200human GRCh38 chrX: 54,225,734-54,225,734 , GRCh38 chrX: 54,225,798-54,225,798 , GRCh37.p13 chrX: 54,252,167-54,252,167 , GRCh37.p13 chrX: 54,252,231-54,252,231 , GRCh37.p13 chrX|NW_004070877.1: 3,938,849-3,938,849 , GRCh37.p13 chrX|NW_004070877.1: 3,938,913-3,938,913 WNK3
    nsv5332142translocation1nstd200human GRCh37 chrX: 54,218,931-54,218,931 , GRCh37 chrX: 54,218,881-54,218,881 , GRCh38.p12 chrX: 54,192,498-54,192,498 , GRCh38.p12 chrX: 54,192,448-54,192,448 WNK3
    nsv5197861mobile element insertion1nstd203human GRCh38 chrX: 54,301,088-54,301,093 , GRCh37.p13 chrX|NW_004070877.1: 4,014,203-4,014,208 , GRCh37.p13 chrX: 54,327,521-54,327,526 WNK3
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