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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
    nsv5886594copy number variation1nstd209human GRCh38 chrX: 101,836,460-101,836,546 , GRCh37.p13 chrX: 101,091,432-101,091,518 NXF5
    nsv5672496copy number variation1nstd207human GRCh38 chrX: 101,836,460-101,836,546 , GRCh37.p13 chrX: 101,091,432-101,091,518 NXF5
    nsv5672279copy number variation1nstd207human GRCh38 chrX: 101,834,921-101,835,176 , GRCh37.p13 chrX: 101,089,894-101,090,149 NXF5
    nsv5668434copy number variation1nstd207human GRCh38 chrX: 101,835,677-101,835,928 , GRCh37.p13 chrX: 101,090,650-101,090,901 NXF5
    nsv5667554copy number variation1nstd207human GRCh38 chrX: 101,842,234-101,842,704 , GRCh37.p13 chrX: 101,097,206-101,097,676 NXF5
    nsv5419433copy number variation1nstd206human GRCh38 chrX: 101,851,755-101,854,167 , GRCh37.p13 chrX: 101,106,727-101,109,139 NXF5
    nsv5376800translocation1nstd200human GRCh38 chrX: 101,836,548-101,836,548 , GRCh38 chrX: 101,836,460-101,836,460 , GRCh37.p13 chrX: 101,091,520-101,091,520 , GRCh37.p13 chrX: 101,091,432-101,091,432 NXF5
    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
    nsv4779900copy number variation1nstd200human GRCh37 chrX: 101,091,432-101,091,520 , GRCh38.p12 chrX: 101,836,460-101,836,548 NXF5
    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
    nsv4764340copy number variation1nstd199human GRCh37 chrX: 101,091,431-101,091,518 , GRCh38.p12 chrX: 101,836,459-101,836,546 NXF5
    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
    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
    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
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