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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5562609sequence alteration1nstd206human GRCh38 chr18: 35,234,158-35,343,147 , GRCh37.p13 chr18: 32,814,122-32,923,111 , ZNF24, 3 more genes
    nsv5522994copy number variation1nstd206human GRCh38 chr18: 35,331,630-35,331,883 , GRCh37.p13 chr18: 32,911,594-32,911,847 , ZNF24
    nsv5375166translocation1nstd200human GRCh38 chr18: 35,254,047-35,254,047 , GRCh38 chr18: 35,343,147-35,343,147 , GRCh37.p13 chr18: 32,923,111-32,923,111 , GRCh37.p13 chr18: 32,834,011-32,834,011 ZNF24, ZNF397, 1 more genes
    nsv5340239translocation1nstd200human GRCh37 chr18: 32,923,111-32,923,111 , GRCh37 chr18: 32,834,011-32,834,011 , GRCh38.p12 chr18: 35,254,047-35,254,047 , GRCh38.p12 chr18: 35,343,147-35,343,147 ZNF24, ZNF397, 1 more genes
    nsv5291743copy number variation1nstd204human GRCh38.p13 chr18: 35,344,401-35,350,400 , GRCh37.p13 chr18: 32,924,365-32,930,364 ZNF24
    nsv5036576inversion1nstd200human GRCh38 chr18: 33,011,377-36,071,277 , GRCh37.p13 chr18: 30,591,341-33,651,240 , ZSCAN30, 25 more genes
    nsv4871565inversion1nstd200human GRCh37 chr18: 30,591,341-33,651,241 , GRCh38.p12 chr18: 33,011,377-36,071,278 , LOC105372066, 25 more genes
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
    nsv4676233copy number variation1nstd102humanPathogenic GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790 DHFRP1, CLUHP6, 116 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4262024copy number variation1nstd166human GRCh37.p13 chr18: 32,911,594-32,911,847 , GRCh38.p12 chr18: 35,331,630-35,331,883 , ZNF24
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
    nsv3923838copy number variation1nstd102humanPathogenic NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381 WDR7-OT1, HMGN1P30, 941 more genes
    nsv3921154copy number variation1nstd102humanUncertain significance NCBI36 chr18: 30,288,042-31,589,339 , GRCh38 chr18: 34,454,080-35,755,377 , GRCh37 chr18: 32,034,044-33,335,341 MAPRE2, LOC105372065, 14 more genes
    nsv3920818copy number variation1nstd102humanPathogenic NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298 AQP4-AS1, SERPINB8, 670 more genes
    nsv3920302copy number variation1nstd102humanPathogenic NCBI36 chr18: 29,881,080-37,228,316 , GRCh38 chr18: 34,047,118-41,394,354 , GRCh37 chr18: 31,627,082-38,974,318 FHOD3, MIR3975, 61 more genes
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