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Items: 1 to 20 of 282

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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
    nsv5730974mobile element insertion1nstd211human GRCh38 chrX: 111,894,029-111,894,029 , GRCh37.p13 chrX: 111,137,257-111,137,257 TRPC5, TRPC5OS
    nsv5555883mobile element insertion1nstd206human GRCh38 chrX: 111,894,029-111,894,080 , GRCh37.p13 chrX: 111,137,257-111,137,308 TRPC5, TRPC5OS
    nsv5415436copy number variation1nstd206human GRCh38 chrX: 111,890,526-111,890,588 , GRCh37.p13 chrX: 111,133,754-111,133,816 TRPC5, TRPC5OS
    nsv5376881translocation1nstd200human GRCh38 chrX: 111,890,588-111,890,588 , GRCh38 chrX: 111,890,526-111,890,526 , GRCh37.p13 chrX: 111,133,816-111,133,816 , GRCh37.p13 chrX: 111,133,754-111,133,754 TRPC5, TRPC5OS
    nsv5336363translocation1nstd200human GRCh37 chrX: 111,133,754-111,133,754 , GRCh37 chrX: 111,133,816-111,133,816 , GRCh38.p12 chrX: 111,890,526-111,890,526 , GRCh38.p12 chrX: 111,890,588-111,890,588 TRPC5OS, TRPC5
    nsv5161985mobile element insertion1nstd203human GRCh38 chrX: 111,874,053-111,874,069 , GRCh37.p13 chrX: 111,117,281-111,117,297 TRPC5, TRPC5OS
    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
    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
    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
    nsv4637600copy number variation1nstd186human GRCh37 chrX: 111,133,754-111,133,816 , GRCh38.p12 chrX: 111,890,526-111,890,588 TRPC5OS, TRPC5
    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
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