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Items: 1 to 20 of 263

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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
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    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
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4779892copy number variation1nstd200human GRCh37 chrX: 100,596,107-100,598,985 , GRCh38.p12 chrX: 101,341,119-101,343,997 TIMM8A, RPL21P132
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4685584copy number variation1nstd102humanPathogenic GRCh37 chrX: 100,601,463-100,603,745 , GRCh38.p12 chrX: 101,346,475-101,348,757 BTK, TIMM8A
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4674310copy number variation1nstd102humanUncertain significance GRCh37 chrX: 99,910,467-100,704,219 , GRCh38.p12 chrX: 100,655,470-101,449,231 HNRNPA1P27, PPIAP89, 27 more genes
    nsv4674080copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,387,417-155,233,731 , GRCh38.p12 chrX: 85,132,411-156,004,066 CSTF2, GPR119, 1029 more genes
    nsv4578479copy number variation1nstd102humanUncertain significance GRCh37 chrX: 100,183,898-100,809,683 , GRCh38.p12 chrX: 100,928,909-101,554,700 ARMCX1, RNU6-934P, 20 more genes
    nsv4452492copy number variation1nstd102humanPathogenic GRCh37 chrX: 58,455,352-155,233,731 , GRCh38.p12 chrX: 58,428,919-156,004,066 RNU6-122P, LOC100421910, 1347 more genes
    nsv4452442copy number variation1nstd102humanPathogenic GRCh37 chrX: 92,814,516-155,233,731 , GRCh38.p12 chrX: 93,559,517-156,004,066 TEX13D, CT45A5, 978 more genes
    nsv4452339copy number variation1nstd102humanUncertain significance GRCh37 chrX: 99,858,358-100,772,721 , GRCh38.p12 chrX: 100,603,361-101,517,734 RPL36A-HNRNPH2, PPIAP89, 29 more genes
    nsv4450523copy number variation1nstd102humanUncertain significance GRCh37 chrX: 54,941,868-155,233,731 , GRCh38.p12 chrX: 54,915,435-156,004,066 LOC105373348, MIR548AN, 1396 more genes
    nsv4380296copy number variation3nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , RPL31P63, 2192 more genes
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