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Items: 1 to 20 of 260

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5716943mobile element insertion1nstd211human GRCh38 chrX: 136,494,190-136,494,190 , GRCh37.p13 chrX: 135,576,349-135,576,349 BRS3
    nsv5562174mobile element insertion1nstd206human GRCh38 chrX: 136,494,190-136,494,241 , GRCh37.p13 chrX: 135,576,349-135,576,400 BRS3
    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
    nsv5041083inversion1nstd200human GRCh38 chrX: 136,450,318-138,402,964 , GRCh37.p13 chrX: 135,532,477-137,485,123 SRRM1P3, TM9SF5P, 23 more genes
    nsv4909170copy number variation1nstd200human GRCh38 chrX: 136,487,316-136,507,577 , GRCh37.p13 chrX: 135,569,475-135,589,736 BRS3, HTATSF1
    nsv4872387inversion1nstd200human GRCh37 chrX: 135,532,477-137,485,129 , GRCh38.p12 chrX: 136,450,318-138,402,970 SNORD61, CD40LG, 23 more genes
    nsv4782362copy number variation1nstd200human GRCh37 chrX: 135,569,440-135,589,765 , GRCh38.p12 chrX: 136,487,281-136,507,606 BRS3, HTATSF1
    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
    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
    nsv4728472copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,190,085-135,599,019 , GRCh38.p12 chrX: 136,107,926-136,516,860 MAP7D3, BRS3, 4 more genes
    nsv4685620copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551 ABCD1, AMD1P2, 560 more genes
    nsv4679893copy number variation1nstd189human GRCh37.p13 chrX: 113,759,648-150,222,670 , GRCh38.p12 chrX: 114,525,195-151,054,198 , AGTR2, 532 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
    nsv4578241copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,757,437-155,208,244 , GRCh38.p12 chrX: 123,623,586-155,978,579 ABCD1, AMD1P2, 557 more genes
    nsv4575216mobile element insertion1nstd166human GRCh37.p13 chrX: 135,575,583-135,575,583 , GRCh38.p12 chrX: 136,493,424-136,493,424 BRS3
    nsv4454214copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,924,044-155,233,731 , GRCh38.p12 chrX: 123,790,194-156,004,066 LOC107985666, FLNA, 555 more genes
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