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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
    nsv7082299copy number variation1nstd229human GRCh38 chrX: 110,176,881-110,177,184 , GRCh37.p13 chrX: 109,420,109-109,420,412 TMEM164
    nsv7082298copy number variation1nstd229human GRCh38 chrX: 110,162,356-110,168,028 , GRCh37.p13 chrX: 109,405,584-109,411,256 TMEM164
    nsv7082297copy number variation1nstd229human GRCh38 chrX: 110,154,981-110,158,175 , GRCh37.p13 chrX: 109,398,209-109,401,403 TMEM164
    nsv7082296copy number variation1nstd229human GRCh38 chrX: 110,150,328-110,154,351 , GRCh37.p13 chrX: 109,393,556-109,397,579 TMEM164
    nsv7082295copy number variation1nstd229human GRCh38 chrX: 110,147,666-110,458,509 , GRCh37.p13 chrX: 109,390,894-109,701,737 LOC105373312, SNORD96B, 4 more genes
    nsv7082294copy number variation1nstd229human GRCh38 chrX: 110,147,050-110,152,754 , GRCh37.p13 chrX: 109,390,278-109,395,982 TMEM164
    nsv7082293copy number variation1nstd229human GRCh38 chrX: 110,141,249-110,151,010 , GRCh37.p13 chrX: 109,384,477-109,394,238 TMEM164
    nsv7082292copy number variation1nstd229human GRCh38 chrX: 110,134,494-110,134,642 , GRCh37.p13 chrX: 109,377,722-109,377,870 TMEM164
    nsv7082291copy number variation1nstd229human GRCh38 chrX: 110,124,290-110,131,922 , GRCh37.p13 chrX: 109,367,518-109,375,150 TMEM164
    nsv7082290copy number variation1nstd229human GRCh38 chrX: 110,114,334-110,119,282 , GRCh37.p13 chrX: 109,357,562-109,362,510 TMEM164
    nsv7082289copy number variation1nstd229human GRCh38 chrX: 110,106,214-110,106,323 , GRCh37.p13 chrX: 109,349,442-109,349,551 TMEM164
    nsv7082288copy number variation1nstd229human GRCh38 chrX: 110,105,590-110,108,636 , GRCh37.p13 chrX: 109,348,818-109,351,864 TMEM164
    nsv7082287copy number variation1nstd229human GRCh38 chrX: 110,081,946-110,086,467 , GRCh37.p13 chrX: 109,325,174-109,329,695 TMEM164, MIR3978
    nsv7082286copy number variation1nstd229human GRCh38 chrX: 110,081,118-110,084,379 , GRCh37.p13 chrX: 109,324,346-109,327,607 MIR3978, TMEM164
    nsv7082285copy number variation1nstd229human GRCh38 chrX: 110,076,430-110,077,516 , GRCh37.p13 chrX: 109,319,658-109,320,744 TMEM164
    nsv7082284copy number variation1nstd229human GRCh38 chrX: 110,070,789-110,094,563 , GRCh37.p13 chrX: 109,314,017-109,337,791 TMEM164, MIR3978
    nsv7082283copy number variation1nstd229human GRCh38 chrX: 110,053,601-110,059,400 , GRCh37.p13 chrX: 109,296,829-109,302,628 MIR652, TMEM164
    nsv7082282copy number variation1nstd229human GRCh38 chrX: 110,033,991-110,040,413 , GRCh37.p13 chrX: 109,277,219-109,283,641 TMEM164
    nsv7082281copy number variation1nstd229human GRCh38 chrX: 110,021,346-110,048,203 , GRCh37.p13 chrX: 109,264,574-109,291,431 TMEM164
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