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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 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
    nsv5979109copy number variation1nstd209human GRCh38 chrX: 154,525,030-154,539,295 , GRCh37.p13 chrX|NW_003871103.3: 1,959,009-1,973,274 , GRCh37.p13 chrX: 153,753,248-153,767,509 G6PD, IKBKG
    nsv5977827copy number variation1nstd209human GRCh38 chrX: 154,546,527-154,558,726 , GRCh37.p13 chrX|NW_003871103.3: 1,980,506-1,992,705 , GRCh37.p13 chrX: 153,774,742-153,786,941 IKBKG, G6PD
    nsv5724390mobile element insertion1nstd211human GRCh38 chrX: 154,539,035-154,539,035 , GRCh37.p13 chrX|NW_003871103.3: 1,973,014-1,973,014 , GRCh37.p13 chrX: 153,767,249-153,767,249 G6PD
    nsv5558972mobile element insertion1nstd206human GRCh38 chrX: 154,539,035-154,539,086 , GRCh37.p13 chrX: 153,767,249-153,767,300 , GRCh37.p13 chrX|NW_003871103.3: 1,973,014-1,973,065 G6PD
    nsv5432224copy number variation1nstd206human GRCh38 chrX: 154,537,059-154,537,136 , GRCh37.p13 chrX|NW_003871103.3: 1,971,038-1,971,115 , GRCh37.p13 chrX: 153,765,274-153,765,351 G6PD
    nsv5381712copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,760,215-153,775,961 , GRCh38.p12 chrX: 154,532,000-154,547,746 G6PD, IKBKG
    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
    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
    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
    nsv4560441mobile element insertion1nstd166human GRCh37.p13 chrX: 153,767,235-153,767,235 , GRCh38.p12 chrX: 154,539,021-154,539,021 G6PD
    nsv4518258copy number variation1nstd166human GRCh37.p13 chrX: 153,722,399-154,023,000 , GRCh38.p12 chrX: 154,494,053-154,794,725 G6PD, MPP1, 18 more genes
    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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