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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
    nsv5970888copy number variation1nstd209human GRCh37.p13 chrX|NW_004070890.2: 5,453,889-5,474,272 , GRCh38 chrX: 149,929,491-149,949,874 , GRCh37.p13 chrX: 149,097,709-149,118,092 EOLA2-DT, HSFX4, 1 more genes
    nsv5557365sequence alteration1nstd206human GRCh37.p13 chrX|NW_004070890.2: 5,059,217-5,469,910 , GRCh38 chrX: 149,534,819-149,945,512 , GRCh37.p13 chrX: 148,616,351-149,113,730 MAGEA9, HSFX2, 19 more genes
    nsv5424262copy number variation1nstd206human GRCh37.p13 chrX|NW_004070890.2: 5,453,398-5,866,004 , GRCh38 chrX: 149,929,000-150,341,606 , GRCh37.p13 chrX: 149,097,218-149,509,861 XRCC6P2, EOLA2, 4 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
    nsv4782431copy number variation1nstd200human GRCh37 chrX: 148,769,378-149,527,672 , GRCh38.p12 chrX: 149,687,712-150,359,419 MAGEA7P, LOC643015, 15 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
    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
    nsv4684033copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 148,882,560-149,686,856 , GRCh38.p12 chrX: 149,800,898-150,518,587 MAGEA7P, MAGEA8, 10 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
    nsv4673988copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,972,739-149,446,095 , GRCh38.p12 chrX: 149,843,927-150,277,877 XRCC6P2, MIR2114, 7 more genes
    nsv4637065copy number variation4nstd186human GRCh37 chrX: 149,088,900-149,094,150 , GRCh38.p12 chrX: 149,920,682-149,925,932 EOLA2
    nsv4629208copy number variation1nstd183human GRCh37 chrX: 149,107,022-149,109,390 , GRCh38.p12 chrX: 149,938,804-149,941,172 EOLA2, EOLA2-DT
    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
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