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Items: 1 to 20 of 327

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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
    nsv7097988copy number variation1nstd102humanUncertain significance GRCh37 chrX: 128,674,417-128,975,921 , GRCh38.p12 chrX: 129,540,440-129,841,945 XPNPEP2, SASH3, 4 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
    nsv7079028copy number variation1nstd229human GRCh38 chrX: 129,838,864-129,839,113 , GRCh37.p13 chrX: 128,972,840-128,973,089 ZDHHC9
    nsv7079027copy number variation1nstd229human GRCh38 chrX: 129,804,155-129,806,205 , GRCh37.p13 chrX: 128,938,131-128,940,181 ZDHHC9
    nsv7050070inversion1nstd229human GRCh38 chrX: 129,842,384-129,844,967 , GRCh37.p13 chrX: 128,976,360-128,978,943 ZDHHC9
    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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137579copy number variation1nstd213human GRCh37 chrX: 114,940,000-134,860,001 , GRCh38.p12 chrX: 115,705,680-135,719,285 AGTR2, SLC25A5, 295 more genes
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
    nsv6137362copy number variation1nstd213human GRCh37 chrX: 104,480,000-134,870,001 , GRCh38.p12 chrX: 105,235,316-135,719,285 AGTR2, SLC25A5, 423 more genes
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