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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
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5884570copy number variation1nstd209human GRCh38 chrX: 147,912,049-147,912,108 , GRCh37.p13 chrX|NW_004070890.2: 3,436,440-3,436,499 , GRCh37.p13 chrX: 146,993,567-146,993,626 FMR1, FMR1-AS1
    nsv5613858insertion1nstd207human GRCh38 chrX: 147,912,049-147,912,049 , GRCh37.p13 chrX: 146,993,567-146,993,567 , GRCh37.p13 chrX|NW_004070890.2: 3,436,440-3,436,440 FMR1, FMR1-AS1
    nsv5169002mobile element insertion1nstd203human GRCh38 chrX: 147,918,259-147,918,269 , GRCh37.p13 chrX: 146,999,777-146,999,787 , GRCh37.p13 chrX|NW_004070890.2: 3,442,650-3,442,660 FMR1
    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
    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
    nsv4757423insertion1nstd199human GRCh37 chrX: 146,993,558-146,993,558 , GRCh38.p12 chrX: 147,912,040-147,912,040 FMR1, FMR1-AS1
    nsv4728768copy number variation1nstd102humanUncertain significance GRCh37 chrX: 146,634,335-147,115,161 , GRCh38.p12 chrX: 147,552,817-148,033,641 RNA5SP524, LOC105373349, 5 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
    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
    nsv4571712mobile element insertion1nstd166human GRCh37.p13 chrX: 146,998,078-146,998,078 , GRCh38.p12 chrX: 147,916,560-147,916,560 FMR1
    nsv4567307mobile element insertion1nstd166human GRCh37.p13 chrX: 146,999,777-146,999,777 , GRCh38.p12 chrX: 147,918,259-147,918,259 FMR1
    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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