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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
    nsv7098222copy number variation1nstd102humanPathogenic GRCh37 chrX: 128,674,417-129,299,630 , GRCh38.p12 chrX: 129,540,440-130,165,656 LOC105373334, ZDHHC9, 11 more genes
    nsv7079047copy number variation1nstd229human GRCh38 chrX: 130,058,101-130,110,600 , GRCh37.p13 chrX: 129,192,076-129,244,575 RAB33A, ELF4, 1 more genes
    nsv7079046copy number variation1nstd229human GRCh38 chrX: 130,055,819-130,069,647 , GRCh37.p13 chrX: 129,189,794-129,203,622 BCORL1, ELF4
    nsv7079045copy number variation1nstd229human GRCh38 chrX: 130,052,066-130,052,262 , GRCh37.p13 chrX: 129,186,041-129,186,237 BCORL1
    nsv7079044copy number variation1nstd229human GRCh38 chrX: 130,035,107-130,035,306 , GRCh37.p13 chrX: 129,169,082-129,169,281 BCORL1
    nsv7079043copy number variation1nstd229human GRCh38 chrX: 130,014,727-130,014,906 , GRCh37.p13 chrX: 129,148,703-129,148,882 BCORL1
    nsv7079042copy number variation1nstd229human GRCh38 chrX: 129,997,393-130,070,457 , GRCh37.p13 chrX: 129,131,369-129,204,432 ELF4, BCORL1
    nsv7079041copy number variation1nstd229human GRCh38 chrX: 129,991,372-129,993,872 , GRCh37.p13 chrX: 129,125,348-129,127,848 BCORL1
    nsv7079040copy number variation1nstd229human GRCh38 chrX: 129,980,301-130,072,900 , GRCh37.p13 chrX: 129,114,277-129,206,875 ELF4, BCORL1
    nsv7079039copy number variation1nstd229human GRCh38 chrX: 129,978,901-129,983,100 , GRCh37.p13 chrX: 129,112,877-129,117,076 BCORL1
    nsv7079035copy number variation1nstd229human GRCh38 chrX: 129,935,901-130,143,300 , GRCh37.p13 chrX: 129,069,877-129,277,275 AIFM1, RAB33A, 3 more genes
    nsv7079029copy number variation1nstd229human GRCh38 chrX: 129,840,501-130,149,500 , GRCh37.p13 chrX: 128,974,477-129,283,475 BCORL1, UTP14A, 6 more genes
    nsv7042777inversion1nstd229human GRCh38 chrX: 127,009,007-134,341,039 , GRCh37.p13 chrX: 126,142,990-133,475,069 ELF4, TJAP1P1, 97 more genes
    nsv6636493copy number variation1nstd102humanUncertain significance GRCh37 chrX: 127,753,972-129,202,285 , GRCh38.p12 chrX: 128,619,994-130,068,310 LOC107985684, UTP14A, 18 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 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
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