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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
    nsv5945682copy number variation1nstd209human GRCh38 chr18: 26,693,662-26,693,746 , GRCh37.p13 chr18: 24,273,626-24,273,710 PCAT18
    nsv5711696mobile element insertion2nstd211human GRCh38 chr18: 26,702,624-26,702,624 , GRCh37.p13 chr18: 24,282,588-24,282,588 PCAT18
    nsv5695364mobile element insertion2nstd211human GRCh38 chr18: 26,688,614-26,688,614 , GRCh37.p13 chr18: 24,268,578-24,268,578 PCAT18, LOC102725227
    nsv5428877mobile element insertion1nstd206human GRCh38 chr18: 26,688,614-26,688,665 , GRCh37.p13 chr18: 24,268,578-24,268,629 LOC102725227, PCAT18
    nsv5146641mobile element insertion1nstd203human GRCh38 chr18: 26,702,613-26,702,624 , GRCh37.p13 chr18: 24,282,577-24,282,588 PCAT18
    nsv5142695mobile element insertion1nstd203human GRCh38 chr18: 26,688,604-26,688,614 , GRCh37.p13 chr18: 24,268,568-24,268,578 PCAT18, LOC102725227
    nsv4729865copy number variation1nstd102humanUncertain significance GRCh37 chr18: 23,586,307-25,193,192 , GRCh38.p12 chr18: 26,006,343-27,613,228 ATP6V1E1P2, SINHCAFP1, 29 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
    nsv4502941mobile element insertion1nstd166human GRCh37.p13 chr18: 24,268,568-24,268,568 , GRCh38.p12 chr18: 26,688,604-26,688,604 PCAT18, LOC102725227
    nsv4499333mobile element insertion1nstd166human GRCh37.p13 chr18: 24,282,577-24,282,577 , GRCh38.p12 chr18: 26,702,613-26,702,613 PCAT18
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    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
    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
    nsv3920487copy number variation1nstd102humanPathogenic NCBI36 chr18: 16,783,337-30,197,417 , GRCh38 chr18: 20,949,378-34,363,455 , GRCh37 chr18: 18,529,339-31,943,419 CCDC178, RNA5SP452, 159 more genes
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