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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6113709copy number variation1nstd186human GRCh37 chrX: 110,558,111-110,559,334 , GRCh38.p12 chrX: 111,314,883-111,316,106 DCX
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5972313copy number variation1nstd209human GRCh38 chrX: 111,343,298-111,348,597 , GRCh37.p13 chrX: 110,586,526-110,591,825 DCX
    nsv5883290copy number variation1nstd209human GRCh38 chrX: 111,342,955-111,371,807 , GRCh37.p13 chrX: 110,586,183-110,615,035 DCX
    nsv5871123copy number variation1nstd209human GRCh38 chrX: 111,314,868-111,316,105 , GRCh37.p13 chrX: 110,558,096-110,559,333 DCX
    nsv5665885copy number variation1nstd207human GRCh38 chrX: 111,352,616-111,352,712 , GRCh37.p13 chrX: 110,595,844-110,595,940 DCX
    nsv5432766copy number variation1nstd206human GRCh38 chrX: 111,329,131-111,329,435 , GRCh37.p13 chrX: 110,572,359-110,572,663 DCX
    nsv5424979copy number variation1nstd206human GRCh38 chrX: 111,352,616-111,352,713 , GRCh37.p13 chrX: 110,595,844-110,595,941 DCX
    nsv5423202copy number variation1nstd206human GRCh38 chrX: 111,314,883-111,316,106 , GRCh37.p13 chrX: 110,558,111-110,559,334 DCX
    nsv5393629mobile element deletion1nstd186human GRCh37 chrX: 110,558,112-110,559,401 , GRCh38.p12 chrX: 111,314,884-111,316,173 DCX
    nsv5393621mobile element deletion1nstd186human GRCh37 chrX: 110,558,111-110,559,334 , GRCh38.p12 chrX: 111,314,883-111,316,106 DCX
    nsv5376879translocation1nstd200human GRCh38 chrX: 111,383,648-111,383,648 , GRCh38 chrX: 111,383,740-111,383,740 , GRCh37.p13 chrX: 110,626,968-110,626,968 , GRCh37.p13 chrX: 110,626,876-110,626,876 DCX
    nsv5376878translocation1nstd200human GRCh38 chrX: 111,329,131-111,329,131 , GRCh38 chrX: 111,329,435-111,329,435 , GRCh37.p13 chrX: 110,572,663-110,572,663 , GRCh37.p13 chrX: 110,572,359-110,572,359 DCX
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5036543mobile element deletion1nstd200human GRCh38 chrX: 111,314,883-111,316,106 , GRCh37.p13 chrX: 110,558,111-110,559,334 DCX
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905856copy number variation1nstd200human GRCh38 chrX: 111,318,219-111,330,817 , GRCh37.p13 chrX: 110,561,447-110,574,045 DCX
    nsv4884050mobile element deletion1nstd200human GRCh37 chrX: 110,558,109-110,559,402 , GRCh38.p12 chrX: 111,314,881-111,316,174 DCX
    nsv4782253copy number variation1nstd200human GRCh37 chrX: 110,561,447-110,574,045 , GRCh38.p12 chrX: 111,318,219-111,330,817 DCX
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