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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
    nsv5886529copy number variation1nstd209human GRCh38 chrX: 130,006,606-130,006,816 , GRCh37.p13 chrX: 129,140,582-129,140,792 BCORL1
    nsv5715868mobile element insertion1nstd211human GRCh38 chrX: 130,049,312-130,049,312 , GRCh37.p13 chrX: 129,183,287-129,183,287 BCORL1
    nsv5428419copy number variation1nstd206human GRCh38 chrX: 129,989,241-129,990,405 , GRCh37.p13 chrX: 129,123,217-129,124,381 BCORL1
    nsv5198362mobile element insertion1nstd203human GRCh38 chrX: 130,043,761-130,043,776 , GRCh37.p13 chrX: 129,177,736-129,177,751 BCORL1
    nsv5191667mobile element insertion1nstd203human GRCh38 chrX: 130,043,759-130,043,774 , GRCh37.p13 chrX: 129,177,734-129,177,749 BCORL1
    nsv5185277mobile element insertion1nstd203human GRCh38 chrX: 130,051,032-130,051,042 , GRCh37.p13 chrX: 129,185,007-129,185,017 BCORL1
    nsv5181984mobile element insertion1nstd203human GRCh38 chrX: 130,049,138-130,049,151 , GRCh37.p13 chrX: 129,183,113-129,183,126 BCORL1
    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
    nsv4909131copy number variation1nstd200human GRCh38 chrX: 130,035,107-130,035,306 , GRCh37.p13 chrX: 129,169,082-129,169,281 BCORL1
    nsv4782335copy number variation1nstd200human GRCh37 chrX: 129,169,082-129,169,281 , GRCh38.p12 chrX: 130,035,107-130,035,306 BCORL1
    nsv4780413copy number variation1nstd200human GRCh37 chrX: 129,177,997-129,178,697 , GRCh38.p12 chrX: 130,044,022-130,044,722 BCORL1
    nsv4780412copy number variation1nstd200human GRCh37 chrX: 129,125,298-129,125,838 , GRCh38.p12 chrX: 129,991,322-129,991,862 BCORL1
    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
    nsv4728692copy number variation1nstd102humanPathogenic GRCh37 chrX: 117,120,780-129,850,994 , GRCh38.p12 chrX: 117,986,817-130,717,020 LOC107985709, SLC25A5, 171 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
    nsv4728469copy number variation1nstd102humanUncertain significance GRCh37 chrX: 128,919,362-129,255,906 , GRCh38.p12 chrX: 129,785,386-130,121,931 RAB33A, LOC105373335, 6 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
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