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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
    nsv7098599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,001,546-154,563,736 , GRCh38.p12 chrX: 153,736,092-155,334,427 TAFAZZIN, LOC105373386, 82 more genes
    nsv7098598copy number variation2nstd102humanUncertain significance GRCh37 chrX: 152,014,869-153,363,122 , GRCh38.p12 chrX: 152,846,325-154,097,665 AVPR2, HMGN2P48, 56 more genes
    nsv7098236copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,166,735-153,170,999 , GRCh38.p12 chrX: 153,901,281-153,905,545 AVPR2, ARHGAP4
    nsv7098002copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,128,118-153,664,237 , GRCh38.p12 chrX: 153,862,663-154,435,891 OPN1MW, TEX28, 31 more genes
    nsv7097998copy number variation2nstd102humanUncertain significance GRCh37 chrX: 152,954,030-153,283,591 , GRCh38.p12 chrX: 153,688,575-154,018,140 TMEM187, IDH3G, 21 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7085520copy number variation1nstd229human GRCh38 chrX: 153,389,201-154,074,000 , GRCh37.p13 chrX: 152,654,659-153,339,451 , GRCh37.p13 chrX|NW_003871103.3: 823,184-1,507,979 SLC6A8, PNCK, 39 more genes
    nsv7085519copy number variation1nstd229human GRCh38 chrX: 153,388,501-154,018,300 , GRCh37.p13 chrX|NW_003871103.3: 822,484-1,452,279 , GRCh37.p13 chrX: 152,653,959-153,283,751 RENBP, NAA10, 38 more genes
    nsv7085512copy number variation1nstd229human GRCh38 chrX: 153,378,501-154,041,100 , GRCh37.p13 chrX|NW_003871103.3: 812,484-1,475,079 , GRCh37.p13 chrX: 152,643,959-153,306,551 MIR3202-2, MECP2, 39 more genes
    nsv7079852copy number variation1nstd229human GRCh38 chrX: 153,919,701-153,948,700 , GRCh37.p13 chrX|NW_003871103.3: 1,353,683-1,382,679 , GRCh37.p13 chrX: 153,185,155-153,214,151 HCFC1, RENBP, 2 more genes
    nsv7079851copy number variation1nstd229human GRCh38 chrX: 153,915,462-153,917,121 , GRCh37.p13 chrX: 153,180,916-153,182,575 , GRCh37.p13 chrX|NW_003871103.3: 1,349,444-1,351,103 ARHGAP4
    nsv7079850copy number variation1nstd229human GRCh38 chrX: 153,914,936-153,915,087 , GRCh37.p13 chrX: 153,180,390-153,180,541 , GRCh37.p13 chrX|NW_003871103.3: 1,348,918-1,349,069 ARHGAP4
    nsv7079849copy number variation1nstd229human GRCh38 chrX: 153,914,531-153,916,866 , GRCh37.p13 chrX: 153,179,985-153,182,320 , GRCh37.p13 chrX|NW_003871103.3: 1,348,513-1,350,848 ARHGAP4
    nsv7079848copy number variation1nstd229human GRCh38 chrX: 153,913,201-153,935,900 , GRCh37.p13 chrX|NW_003871103.3: 1,347,183-1,369,881 , GRCh37.p13 chrX: 153,178,655-153,201,353 ARHGAP4, NAA10, 1 more genes
    nsv7079847copy number variation1nstd229human GRCh38 chrX: 153,912,636-153,913,016 , GRCh37.p13 chrX: 153,178,090-153,178,470 , GRCh37.p13 chrX|NW_003871103.3: 1,346,618-1,346,998 ARHGAP4
    nsv7079846copy number variation1nstd229human GRCh38 chrX: 153,908,520-153,908,611 , GRCh37.p13 chrX|NW_003871103.3: 1,342,502-1,342,593 , GRCh37.p13 chrX: 153,173,974-153,174,065 ARHGAP4
    nsv7079845copy number variation1nstd229human GRCh38 chrX: 153,901,601-153,970,300 , GRCh37.p13 chrX|NW_003871103.3: 1,335,583-1,404,279 , GRCh37.p13 chrX: 153,167,055-153,235,751 HCFC1, AVPR2, 4 more genes
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