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Items: 1 to 20 of 285

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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
    nsv5978784copy number variation1nstd209human GRCh38 chrX: 140,010,649-140,018,868 , GRCh37.p13 chrX: 139,092,808-139,101,027 LOC728660
    nsv5970095copy number variation1nstd209human GRCh38 chrX: 140,014,046-140,021,280 , GRCh37.p13 chrX: 139,096,205-139,103,439 LOC728660
    nsv5179614mobile element insertion1nstd203human GRCh38 chrX: 140,016,690-140,016,747 , GRCh37.p13 chrX: 139,098,849-139,098,906 LOC728660
    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
    nsv4728750copy number variation1nstd102humanLikely benign GRCh37 chrX: 138,859,384-139,310,196 , GRCh38.p12 chrX: 139,777,225-140,228,040 MIR505, HNRNPA3P3, 7 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
    nsv4728422copy number variation1nstd102humanUncertain significance GRCh37 chrX: 138,808,850-139,135,113 , GRCh38.p12 chrX: 139,726,691-140,052,954 HNRNPA3P3, ATP11C, 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
    nsv4674340copy number variation1nstd102humanUncertain significance GRCh37 chrX: 138,739,715-139,210,619 , GRCh38.p12 chrX: 139,657,556-140,128,460 ATP11C, MIR505, 8 more genes
    nsv4674302copy number variation1nstd102humanLikely benign GRCh37 chrX: 138,808,850-139,342,599 , GRCh38.p12 chrX: 139,726,691-140,260,434 MIR505, HNRNPA3P3, 7 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
    nsv4518136copy number variation1nstd166human GRCh37.p13 chrX: 138,972,449-139,501,500 , GRCh38.p12 chrX: 139,890,290-140,419,335 EEDP1, ATP11C, 7 more genes
    nsv4517779copy number variation1nstd166human GRCh37.p13 chrX: 138,646,499-139,136,150 , GRCh38.p12 chrX: 139,564,340-140,053,991 BCYRN1P1, MCF2, 6 more genes
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