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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148073copy number variation1nstd102humanUncertain significance GRCh37 chrX: 70,373,327-70,524,150 , GRCh38.p12 chrX: 71,153,477-71,304,300 NONO, NLGN3, 5 more genes
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098673copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,443,558-70,444,409 , GRCh38.p12 chrX: 71,223,708-71,224,559 GJB1
    nsv7098544copy number variation1nstd102humanUncertain significance GRCh37 chrX: 70,327,586-70,683,896 , GRCh38.p12 chrX: 71,107,736-71,464,046 LOC107985688, TAF1, 11 more genes
    nsv7098325copy number variation1nstd102humanUncertain significance GRCh37 chrX: 69,748,945-70,644,108 , GRCh38.p12 chrX: 70,529,095-71,424,258 SOCS5P4, SNX12, 23 more genes
    nsv7088670copy number variation1nstd229human GRCh38 chrX: 71,224,382-71,224,510 , GRCh37.p13 chrX: 70,444,232-70,444,360 GJB1
    nsv7088669copy number variation1nstd229human GRCh38 chrX: 71,215,092-71,220,217 , GRCh37.p13 chrX: 70,434,942-70,440,067 GJB1
    nsv7088668copy number variation1nstd229human GRCh38 chrX: 71,211,660-71,214,794 , GRCh37.p13 chrX: 70,431,510-70,434,644 GJB1
    nsv7088660copy number variation1nstd229human GRCh38 chrX: 71,101,101-71,255,500 , GRCh37.p13 chrX: 70,320,951-70,475,350 LOC107985688, GJB1, 7 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6313346copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,974,855-79,123,671 , GRCh38.p12 chrX: 62,755,385-79,868,171 RPS7P14, RNY4P23, 280 more genes
    nsv6313230copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,877,278-79,123,671 , GRCh38.p12 chrX: 62,657,808-79,868,171 SSBL2P, LOC105373239, 280 more genes
    nsv6293631copy number variation1nstd186human GRCh37 chrX: 70,434,942-70,440,064 , GRCh38.p12 chrX: 71,215,092-71,220,214 GJB1
    nsv6290401copy number variation1nstd102humanUncertain significance GRCh37 chrX: 69,917,640-70,638,292 , GRCh38.p12 chrX: 70,697,790-71,418,442 ZMYM3, GJB1, 23 more genes
    nsv6139106copy number variation1nstd206human GRCh38 chrX: 71,215,092-71,220,214 , GRCh37.p13 chrX: 70,434,942-70,440,064 GJB1
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