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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
    nsv7079215copy number variation1nstd229human GRCh38 chrX: 139,963,637-139,963,770 , GRCh37.p13 chrX: 139,045,796-139,045,929 CXorf66
    nsv7079214copy number variation1nstd229human GRCh38 chrX: 139,961,601-140,004,300 , GRCh37.p13 chrX: 139,043,760-139,086,459 CXorf66
    nsv7079213copy number variation1nstd229human GRCh38 chrX: 139,933,077-140,115,101 , GRCh37.p13 chrX: 139,015,236-139,197,260 CXorf66, LOC728660, 4 more genes
    nsv7079201copy number variation1nstd229human GRCh38 chrX: 139,851,797-140,420,781 , GRCh37.p13 chrX: 138,933,956-139,502,946 EEDP1, RNU6ATAC23P, 8 more genes
    nsv7079198copy number variation1nstd229human GRCh38 chrX: 139,840,259-140,213,866 , GRCh37.p13 chrX: 138,922,418-139,296,018 ATP11C, HNRNPA3P3, 6 more genes
    nsv7079197copy number variation1nstd229human GRCh38 chrX: 139,835,699-140,176,566 , GRCh37.p13 chrX: 138,917,858-139,258,724 HNRNPA3P3, HAPSTR2, 6 more genes
    nsv7079196copy number variation1nstd229human GRCh38 chrX: 139,830,781-140,420,795 , GRCh37.p13 chrX: 138,912,940-139,502,960 MIR505, RNU6ATAC23P, 8 more genes
    nsv7079193copy number variation1nstd229human GRCh38 chrX: 139,818,502-140,054,852 , GRCh37.p13 chrX: 138,900,661-139,137,011 ATP11C, HNRNPA3P3, 4 more genes
    nsv7079192copy number variation1nstd229human GRCh38 chrX: 139,801,458-140,103,777 , GRCh37.p13 chrX: 138,883,617-139,185,936 LOC728660, HAPSTR2, 6 more genes
    nsv7079191copy number variation1nstd229human GRCh38 chrX: 139,769,072-140,369,336 , GRCh37.p13 chrX: 138,851,231-139,451,501 ATP11C, HAPSTR2, 7 more genes
    nsv7079183copy number variation1nstd229human GRCh38 chrX: 139,700,768-139,983,353 , GRCh37.p13 chrX: 138,782,927-139,065,512 BCYRN1P1, MCF2, 4 more genes
    nsv7079149copy number variation1nstd229human GRCh38 chrX: 139,516,644-140,256,830 , GRCh37.p13 chrX: 138,598,803-139,338,995 LOC105373343, F9, 10 more genes
    nsv7079134copy number variation1nstd229human GRCh38 chrX: 139,434,048-142,116,322 , GRCh37.p13 chrX: 138,516,207-141,204,108 LOC101928833, CDR1, 33 more genes
    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
    nsv7079096copy number variation1nstd229human GRCh38 chrX: 139,212,792-142,672,772 , GRCh37.p13 chrX: 138,294,954-141,760,558 ATP11C, LOC105373345, 43 more genes
    nsv7079085copy number variation1nstd229human GRCh38 chrX: 139,139,041-142,300,202 , GRCh37.p13 chrX: 138,221,203-141,387,988 LINC00632, LOC100420230, 40 more genes
    nsv7079081copy number variation1nstd229human GRCh38 chrX: 139,125,994-140,541,920 , GRCh37.p13 chrX: 138,208,156-139,624,085 BCYRN1P1, SRD5A1P1, 17 more genes
    nsv7053951inversion1nstd229human GRCh38 chrX: 139,476,826-140,701,928 , GRCh37.p13 chrX: 138,558,985-139,784,093 CXorf66, MIR505, 15 more genes
    nsv7052075inversion1nstd229human GRCh38 chrX: 139,736,192-140,159,241 , GRCh37.p13 chrX: 138,818,351-139,241,403 CXorf66, MIR505, 6 more genes
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