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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
    nsv7084647copy number variation1nstd229human GRCh38 chrX: 144,305,079-144,329,396 , GRCh37.p13 chrX|NW_004070889.1: 1,093,800-1,118,117 , GRCh37.p13 chrX: 143,388,204-143,412,520 RRM2P4
    nsv7084645copy number variation1nstd229human GRCh38 chrX: 144,298,031-144,404,341 , GRCh37.p13 chrX: 143,381,156-143,487,436 , GRCh37.p13 chrX|NW_004070889.1: 1,086,752-1,193,062 RRM2P4
    nsv7084643copy number variation1nstd229human GRCh38 chrX: 144,296,542-144,312,376 , GRCh37.p13 chrX: 143,379,669-143,395,500 , GRCh37.p13 chrX|NW_004070889.1: 1,085,263-1,101,097 RRM2P4
    nsv7084642copy number variation1nstd229human GRCh38 chrX: 144,282,378-144,403,080 , GRCh37.p13 chrX: 143,365,484-143,486,175 , GRCh37.p13 chrX|NW_004070889.1: 1,071,099-1,191,801 RRM2P4
    nsv7084637copy number variation1nstd229human GRCh38 chrX: 144,260,589-144,626,294 , GRCh37.p13 chrX: 143,343,695-143,707,815 RRM2P4
    nsv7084635copy number variation1nstd229human GRCh38 chrX: 144,244,182-144,491,463 , GRCh37.p13 chrX: 143,327,288-143,573,027 , GRCh37.p13 chrX|NW_004070889.1: 1,032,903-1,214,327 RRM2P4
    nsv7084631copy number variation1nstd229human GRCh38 chrX: 144,214,247-144,392,781 , GRCh37.p13 chrX|NW_004070889.1: 1,002,968-1,181,502 , GRCh37.p13 chrX: 143,297,353-143,475,875 RRM2P4
    nsv7084601copy number variation1nstd229human GRCh38 chrX: 143,830,804-144,422,547 , GRCh37.p13 chrX: 142,913,899-143,505,713 , GRCh37.p13 chrX|NW_004070889.1: 619,525-1,211,268 RRM2P4, UBE2NL
    nsv7079098copy number variation1nstd229human GRCh38 chrX: 139,214,744-145,647,139 , GRCh37.p13 chrX: 138,296,906-142,299,065 LOC101928833, ATP11C, 61 more genes
    nsv7053159inversion1nstd229human GRCh38 chrX: 143,356,368-146,168,320 , GRCh37.p13 chrX|NW_004070890.2: 1-1,692,711 , GRCh37.p13 chrX: 142,444,161-145,249,838 MIR888, MIR890, 22 more genes
    nsv7052188inversion1nstd229human GRCh38 chrX: 143,871,359-146,052,824 , GRCh37.p13 chrX|NW_004070890.2: 1-1,577,215 , GRCh37.p13 chrX: 142,954,450-145,134,342 MIR890, MIR888, 15 more genes
    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
    nsv6637060copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,510,129-145,119,351 , GRCh38.p12 chrX: 140,427,964-146,037,833 LOC101928833, MIR891A, 55 more genes
    nsv6637054copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,493,806-148,855,992 , GRCh38.p12 chrX: 140,411,641-149,774,334 SPANXN4, RRM2P4, 109 more genes
    nsv6636749copy number variation1nstd102humanUncertain significance GRCh37 chrX: 142,414,024-143,403,932 , GRCh38.p12 chrX: 143,326,229-144,320,823 SPANXN3, MTND2P39, 8 more genes
    nsv6636431copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,504,564-149,382,013 , GRCh38.p12 chrX: 140,422,399-150,213,783 MTND1P33, MIR514A1, 119 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
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