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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125225insertion1nstd186human GRCh37 chrX: 83,335,395-83,335,395 , GRCh38.p12 chrX: 84,080,387-84,080,387 RPS6KA6
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5961643insertion1nstd209human GRCh38 chrX: 84,150,852-84,150,852 , GRCh37.p13 chrX: 83,405,860-83,405,860 RPS6KA6
    nsv5955130insertion1nstd209human GRCh38 chrX: 84,080,387-84,080,387 , GRCh37.p13 chrX: 83,335,395-83,335,395 RPS6KA6
    nsv5883469copy number variation1nstd209human GRCh38 chrX: 84,179,584-84,179,665 , GRCh37.p13 chrX: 83,434,592-83,434,673 RPS6KA6
    nsv5725721mobile element insertion1nstd211human GRCh38 chrX: 84,059,613-84,059,613 , GRCh37.p13 chrX: 83,314,621-83,314,621 RPS6KA6
    nsv5723511mobile element insertion1nstd211human GRCh38 chrX: 84,083,528-84,083,528 , GRCh37.p13 chrX: 83,338,536-83,338,536 RPS6KA6
    nsv5717086mobile element insertion1nstd211human GRCh38 chrX: 84,059,624-84,059,624 , GRCh37.p13 chrX: 83,314,632-83,314,632 RPS6KA6
    nsv5623000insertion1nstd207human GRCh38 chrX: 84,150,794-84,150,794 , GRCh37.p13 chrX: 83,405,802-83,405,802 RPS6KA6
    nsv5607396insertion1nstd207human GRCh38 chrX: 84,080,391-84,080,391 , GRCh37.p13 chrX: 83,335,399-83,335,399 RPS6KA6
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5541788insertion1nstd206human GRCh38 chrX: 84,080,387-84,080,387 , GRCh37.p13 chrX: 83,335,395-83,335,395 RPS6KA6
    nsv5427493copy number variation1nstd206human GRCh38 chrX: 84,089,642-84,092,494 , GRCh37.p13 chrX: 83,344,650-83,347,502 RPS6KA6
    nsv5423982copy number variation1nstd206human GRCh38 chrX: 84,177,350-84,179,106 , GRCh37.p13 chrX: 83,432,358-83,434,114 RPS6KA6
    nsv5376621translocation1nstd200human GRCh38 chrX: 84,056,358-84,056,358 , GRCh38 chrX: 84,056,295-84,056,295 , GRCh37.p13 chrX: 83,311,366-83,311,366 , GRCh37.p13 chrX: 83,311,303-83,311,303 RPS6KA6
    nsv5336621translocation1nstd200human GRCh37 chrX: 83,311,303-83,311,303 , GRCh37 chrX: 83,311,366-83,311,366 , GRCh38.p12 chrX: 84,056,295-84,056,295 , GRCh38.p12 chrX: 84,056,358-84,056,358 RPS6KA6
    nsv5177404mobile element insertion1nstd203human GRCh38 chrX: 84,157,468-84,157,480 , GRCh37.p13 chrX: 83,412,476-83,412,488 RPS6KA6
    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
    nsv4908511copy number variation1nstd200human GRCh38 chrX: 84,188,618-84,189,742 , GRCh37.p13 chrX: 83,443,626-83,444,750 RPS6KA6
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