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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124046insertion1nstd186human GRCh37 chrX: 147,843,945-147,843,986 , GRCh38.p12 chrX: 148,762,421-148,762,462 AFF2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5959407insertion1nstd209human GRCh38 chrX: 148,983,953-148,983,953 , GRCh37.p13 chrX|NW_004070890.2: 4,508,350-4,508,350 , GRCh37.p13 chrX: 148,065,483-148,065,483 AFF2
    nsv5956341insertion1nstd209human GRCh38 chrX: 148,772,879-148,772,879 , GRCh37.p13 chrX|NW_004070890.2: 4,297,276-4,297,276 , GRCh37.p13 chrX: 147,854,403-147,854,403 AFF2
    nsv5952305insertion1nstd209human GRCh38 chrX: 148,581,034-148,581,034 , GRCh37.p13 chrX|NW_004070890.2: 4,105,428-4,105,428 , GRCh37.p13 chrX: 147,662,555-147,662,555 AFF2
    nsv5869478copy number variation1nstd209human GRCh38 chrX: 148,772,988-148,776,890 , GRCh37.p13 chrX|NW_004070890.2: 4,297,385-4,301,287 , GRCh37.p13 chrX: 147,854,512-147,858,414 AFF2
    nsv5730308mobile element insertion1nstd211human GRCh38 chrX: 148,725,905-148,725,905 , GRCh37.p13 chrX: 147,807,429-147,807,429 , GRCh37.p13 chrX|NW_004070890.2: 4,250,302-4,250,302 AFF2
    nsv5730132mobile element insertion2nstd211human GRCh38 chrX: 148,588,241-148,588,241 , GRCh37.p13 chrX|NW_004070890.2: 4,112,635-4,112,635 , GRCh37.p13 chrX: 147,669,762-147,669,762 AFF2
    nsv5726963mobile element insertion1nstd211human GRCh38 chrX: 148,971,765-148,971,765 , GRCh37.p13 chrX|NW_004070890.2: 4,496,162-4,496,162 , GRCh37.p13 chrX: 148,053,295-148,053,295 AFF2
    nsv5717051mobile element insertion1nstd211human GRCh38 chrX: 148,642,687-148,642,687 , GRCh37.p13 chrX: 147,724,208-147,724,208 , GRCh37.p13 chrX|NW_004070890.2: 4,167,081-4,167,081 AFF2
    nsv5716506mobile element insertion1nstd211human GRCh38 chrX: 148,795,833-148,795,833 , GRCh37.p13 chrX|NW_004070890.2: 4,320,230-4,320,230 , GRCh37.p13 chrX: 147,877,357-147,877,357 AFF2
    nsv5672219copy number variation1nstd207human GRCh37.p13 chrX|NW_004070890.2: 4,071,533-4,071,609 , GRCh38 chrX: 148,547,139-148,547,215 , GRCh37.p13 chrX: 147,628,660-147,628,736 AFF2
    nsv5669243copy number variation1nstd207human GRCh37.p13 chrX|NW_004070890.2: 4,421,627-4,421,679 , GRCh38 chrX: 148,897,230-148,897,282 , GRCh37.p13 chrX: 147,978,760-147,978,812 AFF2
    nsv5621388insertion1nstd207human GRCh38 chrX: 148,808,828-148,808,828 , GRCh37.p13 chrX: 147,890,352-147,890,352 , GRCh37.p13 chrX|NW_004070890.2: 4,333,225-4,333,225 AFF2
    nsv5620885insertion1nstd207human GRCh38 chrX: 148,581,029-148,581,029 , GRCh37.p13 chrX: 147,662,550-147,662,550 , GRCh37.p13 chrX|NW_004070890.2: 4,105,423-4,105,423 AFF2
    nsv5618945insertion2nstd207human GRCh38 chrX: 148,581,275-148,581,275 , GRCh37.p13 chrX: 147,662,796-147,662,796 , GRCh37.p13 chrX|NW_004070890.2: 4,105,669-4,105,669 AFF2
    nsv5617075insertion1nstd207human GRCh38 chrX: 148,581,249-148,581,249 , GRCh37.p13 chrX: 147,662,770-147,662,770 , GRCh37.p13 chrX|NW_004070890.2: 4,105,643-4,105,643 AFF2
    nsv5615814insertion1nstd207human GRCh38 chrX: 148,581,538-148,581,538 , GRCh37.p13 chrX|NW_004070890.2: 4,105,932-4,105,932 , GRCh37.p13 chrX: 147,663,059-147,663,059 AFF2
    nsv5614672insertion1nstd207human GRCh38 chrX: 148,704,380-148,704,380 , GRCh37.p13 chrX: 147,785,904-147,785,904 , GRCh37.p13 chrX|NW_004070890.2: 4,228,777-4,228,777 AFF2
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