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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 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
    nsv5967156insertion1nstd209human GRCh38 chrX: 101,515,356-101,515,356 , GRCh37.p13 chrX: 100,770,343-100,770,343 , GRCh37.p13 chrX|NW_004070883.1: 197,031-197,031 ARMCX4
    nsv5886969copy number variation1nstd209human GRCh38 chrX: 101,423,160-101,425,709 , GRCh37.p13 chrX|NW_004070883.1: 104,836-107,385 , GRCh37.p13 chrX: 100,678,148-100,680,697 ARMCX4
    nsv5886537copy number variation1nstd209human GRCh38 chrX: 101,433,199-101,433,250 , GRCh37.p13 chrX: 100,688,187-100,688,238 , GRCh37.p13 chrX|NW_004070883.1: 114,875-114,926 ARMCX4
    nsv5872612copy number variation1nstd209human GRCh38 chrX: 101,433,006-101,433,063 , GRCh37.p13 chrX|NW_004070883.1: 114,682-114,739 , GRCh37.p13 chrX: 100,687,994-100,688,051 ARMCX4
    nsv5867889copy number variation1nstd209human GRCh38 chrX: 101,431,564-101,433,434 , GRCh37.p13 chrX: 100,686,552-100,688,422 , GRCh37.p13 chrX|NW_004070883.1: 113,240-115,110 ARMCX4
    nsv5728558mobile element insertion2nstd211human GRCh38 chrX: 101,443,464-101,443,464 , GRCh37.p13 chrX: 100,698,452-100,698,452 , GRCh37.p13 chrX|NW_004070883.1: 125,140-125,140 PPIAP90, ARMCX4
    nsv5722605mobile element insertion1nstd211human GRCh38 chrX: 101,479,323-101,479,323 , GRCh37.p13 chrX|NW_004070883.1: 160,999-160,999 , GRCh37.p13 chrX: 100,734,311-100,734,311 ARMCX4
    nsv5664906copy number variation1nstd207human GRCh37.p13 chrX|NW_004070883.1: 114,877-114,928 , GRCh38 chrX: 101,433,201-101,433,252 , GRCh37.p13 chrX: 100,688,189-100,688,240 ARMCX4
    nsv5623989insertion1nstd207human GRCh38 chrX: 101,515,356-101,515,356 , GRCh37.p13 chrX: 100,770,343-100,770,343 , GRCh37.p13 chrX|NW_004070883.1: 197,031-197,031 ARMCX4
    nsv5619524insertion1nstd207human GRCh38 chrX: 101,494,029-101,494,029 , GRCh37.p13 chrX: 100,749,016-100,749,016 , GRCh37.p13 chrX|NW_004070883.1: 175,704-175,704 ARMCX4
    nsv5618143insertion1nstd207human GRCh38 chrX: 101,433,253-101,433,253 , GRCh37.p13 chrX|NW_004070883.1: 114,929-114,929 , GRCh37.p13 chrX: 100,688,241-100,688,241 ARMCX4
    nsv5614163insertion1nstd207human GRCh38 chrX: 101,433,006-101,433,006 , GRCh37.p13 chrX|NW_004070883.1: 114,682-114,682 , GRCh37.p13 chrX: 100,687,994-100,687,994 ARMCX4
    nsv5433624copy number variation1nstd206human GRCh38 chrX: 101,431,544-101,433,458 , GRCh37.p13 chrX|NW_004070883.1: 113,220-115,134 , GRCh37.p13 chrX: 100,686,532-100,688,446 ARMCX4
    nsv5433617copy number variation1nstd206human GRCh38 chrX: 101,487,449-101,488,304 , GRCh37.p13 chrX|NW_004070883.1: 169,124-169,979 , GRCh37.p13 chrX: 100,742,436-100,743,291 ARMCX4
    nsv5424165copy number variation1nstd206human GRCh38 chrX: 101,423,041-101,425,586 , GRCh37.p13 chrX|NW_004070883.1: 104,717-107,262 , GRCh37.p13 chrX: 100,678,029-100,680,574 ARMCX4
    nsv5415153copy number variation1nstd206human GRCh38 chrX: 101,433,199-101,433,253 , GRCh37.p13 chrX: 100,688,187-100,688,241 , GRCh37.p13 chrX|NW_004070883.1: 114,875-114,929 ARMCX4
    nsv5376799translocation1nstd200human GRCh38 chrX: 101,433,435-101,433,435 , GRCh38 chrX: 101,431,567-101,431,567 , GRCh37.p13 chrX|NW_004070883.1: 113,243-113,243 , GRCh37.p13 chrX: 100,686,555-100,686,555 , GRCh37.p13 chrX: 100,688,423-100,688,423 , GRCh37.p13 chrX|NW_004070883.1: 115,111-115,111 ARMCX4
    nsv5337883translocation1nstd200human GRCh37 chrX: 100,686,555-100,686,555 , GRCh37 chrX: 100,688,423-100,688,423 , GRCh38.p12 chrX: 101,433,435-101,433,435 , GRCh38.p12 chrX: 101,431,567-101,431,567 ARMCX4
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