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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
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7079555copy number variation1nstd229human GRCh38 chrX: 151,700,943-151,706,348 , GRCh37.p13 chrX: 150,869,415-150,874,820 PRRG3
    nsv7079554copy number variation1nstd229human GRCh38 chrX: 151,687,901-151,703,800 , GRCh37.p13 chrX: 150,856,373-150,872,272 PRRG3
    nsv7079553copy number variation1nstd229human GRCh38 chrX: 151,687,801-151,744,900 , GRCh37.p13 chrX: 150,856,273-150,913,372 CNGA2, PRRG3, 1 more genes
    nsv7079552copy number variation1nstd229human GRCh38 chrX: 151,687,801-151,718,100 , GRCh37.p13 chrX: 150,856,273-150,886,572 PRRG3, FATE1
    nsv7079551copy number variation1nstd229human GRCh38 chrX: 151,672,401-151,764,300 , GRCh37.p13 chrX: 150,840,873-150,932,772 CNGA2, FATE1, 2 more genes
    nsv7079550copy number variation1nstd229human GRCh38 chrX: 151,672,201-151,781,600 , GRCh37.p13 chrX: 150,840,673-150,950,072 PASD1, PRRG3, 2 more genes
    nsv7079549copy number variation1nstd229human GRCh38 chrX: 151,654,488-151,712,465 , GRCh37.p13 chrX: 150,822,960-150,880,937 PASD1, PRRG3
    nsv7050820inversion1nstd229human GRCh38 chrX: 143,987,812-153,050,091 , GRCh37.p13 chrX|NW_004070890.2: 1-6,530,008 , GRCh37.p13 chrX: 143,070,918-152,218,449 FMR1NB, MIR4330, 139 more genes
    nsv7046711inversion1nstd229human GRCh38 chrX: 145,641,090-152,809,888 , GRCh37.p13 chrX: 144,722,608-151,978,420 , GRCh37.p13 chrX|NW_004070890.2: 1,165,481-6,530,008 FMR1-AS1, LOC100420321, 126 more genes
    nsv7043638inversion1nstd229human GRCh38 chrX: 145,071,588-152,199,155 , GRCh37.p13 chrX|NW_004070890.2: 595,981-6,530,008 , GRCh37.p13 chrX: 144,153,108-150,174,083 AFF2, CXorf51B, 110 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634391copy number variation1nstd102humanPathogenic GRCh37 chrX: 142,401,540-155,233,731 , GRCh38.p12 chrX: 143,313,746-156,004,066 CSAG4, LOC112268308, 279 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634237copy number variation1nstd224human GRCh37 chrX: 149,422,813-154,913,173 , GRCh38.p12 chrX: 150,254,602-155,683,512 ABCD1, FLNA, 182 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
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