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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098224copy number variation2nstd102humanPathogenic GRCh37 chrX: 12,885,698-13,787,227 , GRCh38.p12 chrX: 12,867,579-13,769,108 GPM6B, MIR6086, 21 more genes
    nsv7097992copy number variation1nstd102humanUncertain significance GRCh37 chrX: 13,734,103-13,787,227 , GRCh38.p12 chrX: 13,715,984-13,769,108 OFD1, TRAPPC2, 1 more genes
    nsv7084349copy number variation1nstd229human GRCh38 chrX: 13,714,887-13,897,966 , GRCh37.p13 chrX: 13,733,006-13,916,085 OFD1, TRAPPC2, 1 more genes
    nsv7079065copy number variation1nstd229human GRCh38 chrX: 13,766,914-13,767,048 , GRCh37.p13 chrX: 13,785,033-13,785,167 OFD1
    nsv7079064copy number variation1nstd229human GRCh38 chrX: 13,731,353-13,733,516 , GRCh37.p13 chrX: 13,749,472-13,751,635 OFD1, TRAPPC2
    nsv7079063copy number variation1nstd229human GRCh38 chrX: 13,705,898-14,295,529 , GRCh37.p13 chrX: 13,724,017-14,313,651 OFD1, RAB9A, 4 more genes
    nsv7077089copy number variation1nstd229human GRCh38 chrX: 13,316,134-13,744,822 , GRCh37.p13 chrX: 13,334,253-13,762,941 TCEANC, RPL30P15, 12 more genes
    nsv7074049copy number variation1nstd229human GRCh38 chrX: 13,221,611-13,939,189 , GRCh37.p13 chrX: 13,239,730-13,957,308 GPX1P1, LINC01203, 14 more genes
    nsv7065917copy number variation1nstd229human GRCh38 chrX: 13,576,583-13,836,181 , GRCh37.p13 chrX: 13,594,702-13,854,300 MIR6086, GPM6B, 8 more genes
    nsv7065809copy number variation1nstd229human GRCh38 chrX: 13,576,583-13,866,779 , GRCh37.p13 chrX: 13,594,702-13,884,898 RN7SKP20, EGFL6, 8 more genes
    nsv7065053copy number variation1nstd229human GRCh38 chrX: 13,552,628-13,802,683 , GRCh37.p13 chrX: 13,570,747-13,820,802 GPM6B, MIR6086, 9 more genes
    nsv7064242copy number variation1nstd229human GRCh38 chrX: 13,115,594-13,744,822 , GRCh37.p13 chrX: 13,133,713-13,762,941 ATXN3L, RPL30P15, 14 more genes
    nsv7064058copy number variation1nstd229human GRCh38 chrX: 13,527,932-13,834,122 , GRCh37.p13 chrX: 13,546,051-13,852,241 MIR6086, LOC107985656, 9 more genes
    nsv7059136copy number variation1nstd229human GRCh38 chrX: 13,684,721-14,295,519 , GRCh37.p13 chrX: 13,702,840-14,313,641 RAB9A, TRAPPC2, 4 more genes
    nsv7023785inversion1nstd229human GRCh38 chrX: 13,472,327-15,761,537 , GRCh37.p13 chrX: 13,490,446-15,779,660 MIR6086, ACE2, 33 more genes
    nsv7019553inversion1nstd229human GRCh38 chrX: 13,770,843-13,770,893 , GRCh37.p13 chrX: 13,788,962-13,789,012 GPM6B, OFD1
    nsv6636165copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899 GPX1P1, XG, 108 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634135copy number variation1nstd224human GRCh37 chrX: 2,700,157-26,836,730 , GRCh38.p12 chrX: 2,782,116-26,818,613 AMELX, ARSF, 258 more genes
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