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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
    nsv5196322mobile element insertion1nstd203human GRCh38 chrX: 153,825,840-153,825,848 , GRCh37.p13 chrX|NW_003871103.3: 1,259,823-1,259,831 , GRCh37.p13 chrX: 153,091,295-153,091,303 PDZD4
    nsv5181520mobile element insertion1nstd203human GRCh38 chrX: 153,825,835-153,825,848 , GRCh37.p13 chrX|NW_003871103.3: 1,259,818-1,259,831 , GRCh37.p13 chrX: 153,091,290-153,091,303 PDZD4
    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
    nsv4787962copy number variation1nstd200human GRCh37 chrX: 153,065,414-153,066,820 , GRCh38.p12 chrX: 153,799,959-153,801,365 PDZD4
    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
    nsv4728727copy number variation1nstd102humanUncertain significance GRCh37 chrX: 152,631,130-153,240,286 , GRCh38.p12 chrX: 153,365,672-153,974,835 ARHGAP4, BCAP31, 34 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
    nsv4681977copy number variation1nstd102humanUncertain significance GRCh37 chrX: 152,954,010-153,141,311 , GRCh38.p12 chrX: 153,688,555-153,875,856 PLXNB3-AS1, SRPK3, 9 more genes
    nsv4681289copy number variation1nstd102humanPathogenic GRCh37 chrX: 152,954,010-153,363,142 , GRCh38.p12 chrX: 153,688,555-154,097,685 NAA10, RENBP, 22 more genes
    nsv4674760copy number variation1nstd102humanPathogenic GRCh37 chrX: 152,516,781-153,368,573 , GRCh38.p12 chrX: 153,251,356-154,103,121 RENBP, TMEM187, 44 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
    nsv4674564copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 153,023,149-153,345,755 , GRCh38.p12 chrX: 153,757,695-154,080,303 ARHGAP4, AVPR2, 19 more genes
    nsv4674212copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,029,046-153,567,369 , GRCh38.p12 chrX: 153,763,591-154,339,019 TEX28P2, LOC105373386, 29 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
    nsv4644850copy number variation1nstd186human GRCh37 chrX: 153,046,775-153,087,962 , GRCh38.p12 chrX: 153,781,320-153,822,507 IDH3G, SSR4, 2 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
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