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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117128copy number variation1nstd186human GRCh37 chrX: 53,135,087-53,137,126 , GRCh38.p12 chrX: 53,105,905-53,107,944 KANTR
    nsv6112721copy number variation1nstd102humanPathogenic GRCh37 chrX: 47,179,068-54,424,785 , GRCh38.p12 chrX: 47,319,669-54,398,352 SNORA11E, SSX11P, 229 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979872copy number variation1nstd209human GRCh38 chrX: 53,105,864-53,108,214 , GRCh37.p13 chrX: 53,135,046-53,137,396 , GRCh37.p13 chrX|NW_004070877.1: 2,818,979-2,821,329 KANTR
    nsv5972606copy number variation1nstd209human GRCh38 chrX: 53,112,115-53,116,414 , GRCh37.p13 chrX|NW_004070877.1: 2,825,230-2,829,529 , GRCh37.p13 chrX: 53,141,297-53,145,596 KANTR
    nsv5884991copy number variation1nstd209human GRCh38 chrX: 53,105,871-53,107,905 , GRCh37.p13 chrX: 53,135,053-53,137,087 , GRCh37.p13 chrX|NW_004070877.1: 2,818,986-2,821,020 KANTR
    nsv5882057copy number variation1nstd209human GRCh38 chrX: 52,862,950-55,652,570 , GRCh37.p13 chrX: 52,891,979-54,424,077 , GRCh37.p13 chrX|NW_004070877.1: 2,576,065-4,110,759 , MIRLET7F2, 64 more genes
    nsv5877794copy number variation1nstd209human GRCh38 chrX: 53,112,594-53,115,586 , GRCh37.p13 chrX: 53,141,776-53,144,768 , GRCh37.p13 chrX|NW_004070877.1: 2,825,709-2,828,701 KANTR
    nsv5725268mobile element insertion1nstd211human GRCh38 chrX: 53,092,750-53,092,750 , GRCh37.p13 chrX|NW_004070877.1: 2,805,865-2,805,865 , GRCh37.p13 chrX: 53,121,932-53,121,932 KANTR
    nsv5672173copy number variation1nstd207human GRCh38 chrX: 53,105,904-53,107,935 , GRCh37.p13 chrX|NW_004070877.1: 2,819,019-2,821,050 , GRCh37.p13 chrX: 53,135,086-53,137,117 KANTR
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5545785insertion1nstd206human GRCh38 chrX: 53,092,750-53,092,794 , GRCh37.p13 chrX: 53,121,932-53,121,976 , GRCh37.p13 chrX|NW_004070877.1: 2,805,865-2,805,909 KANTR
    nsv5421525copy number variation1nstd206human GRCh38 chrX: 53,105,905-53,107,944 , GRCh37.p13 chrX|NW_004070877.1: 2,819,020-2,821,059 , GRCh37.p13 chrX: 53,135,087-53,137,126 KANTR
    nsv5419529copy number variation1nstd206human GRCh38 chrX: 53,108,231-53,111,076 , GRCh37.p13 chrX|NW_004070877.1: 2,821,346-2,824,191 , GRCh37.p13 chrX: 53,137,413-53,140,258 KANTR
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5384070copy number variation1nstd186human GRCh37 chrX: 53,135,098-53,137,071 , GRCh38.p12 chrX: 53,105,916-53,107,889 KANTR
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905511copy number variation1nstd200human GRCh38 chrX: 53,103,119-53,104,512 , GRCh37.p13 chrX|NW_004070877.1: 2,816,234-2,817,627 , GRCh37.p13 chrX: 53,132,301-53,133,694 KANTR
    nsv4902713copy number variation1nstd200human GRCh38 chrX: 53,113,520-53,113,575 , GRCh37.p13 chrX|NW_004070877.1: 2,826,635-2,826,690 , GRCh37.p13 chrX: 53,142,702-53,142,757 KANTR
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