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Items: 1 to 20 of 943

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139626copy number variation1nstd232human GRCh37.p13 chr18: 53,288,738-53,288,915 , GRCh38.p12 chr18: 55,621,507-55,621,684 TCF4
    nsv7095447copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,017,570-53,254,347 , GRCh38.p12 chr18: 55,350,339-55,587,116 TCF4, MIR4529, 1 more genes
    nsv7095386copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,017,570-53,070,769 , GRCh38.p12 chr18: 55,350,339-55,403,538 TCF4
    nsv7095385copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,927,160-53,254,347 , GRCh38.p12 chr18: 55,259,929-55,587,116 MIR4529, TCF4-AS1, 1 more genes
    nsv7095251copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,128,230-53,131,388 , GRCh38.p12 chr18: 55,460,999-55,464,157 TCF4, TCF4-AS1
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7066250inversion1nstd229human GRCh38 chr18: 54,862,924-58,506,448 , GRCh37.p13 chr18: 52,530,155-56,173,680 NARS1, FECH, 48 more genes
    nsv7017944copy number variation1nstd229human GRCh38 chr18: 55,431,399-55,434,902 , GRCh37.p13 chr18: 53,098,630-53,102,133 TCF4
    nsv7017344copy number variation1nstd229human GRCh38 chr18: 55,357,096-55,369,737 , GRCh37.p13 chr18: 53,024,327-53,036,968 TCF4
    nsv7016701copy number variation1nstd229human GRCh38 chr18: 55,618,921-55,822,158 , GRCh37.p13 chr18: 53,286,152-53,489,389 LOC105372130, RPL21P126, 2 more genes
    nsv7015979copy number variation1nstd229human GRCh38 chr18: 55,603,337-55,608,878 , GRCh37.p13 chr18: 53,270,568-53,276,109 TCF4, LOC105372126
    nsv7014357copy number variation1nstd229human GRCh38 chr18: 55,390,447-55,390,489 , GRCh37.p13 chr18: 53,057,678-53,057,720 TCF4
    nsv7014002copy number variation1nstd229human GRCh38 chr18: 55,538,066-55,551,380 , GRCh37.p13 chr18: 53,205,297-53,218,611 TCF4
    nsv7013152copy number variation1nstd229human GRCh38 chr18: 55,384,801-55,392,000 , GRCh37.p13 chr18: 53,052,032-53,059,231 TCF4
    nsv7013151copy number variation1nstd229human GRCh38 chr18: 55,614,655-55,614,761 , GRCh37.p13 chr18: 53,281,886-53,281,992 TCF4
    nsv7012961copy number variation1nstd229human GRCh38 chr18: 55,631,316-55,640,044 , GRCh37.p13 chr18: 53,298,547-53,307,275 RPL21P126, TCF4
    nsv7012411copy number variation1nstd229human GRCh38 chr18: 55,325,246-55,325,414 , GRCh37.p13 chr18: 52,992,477-52,992,645 TCF4
    nsv7010942copy number variation1nstd229human GRCh38 chr18: 55,240,439-55,243,683 , GRCh37.p13 chr18: 52,907,670-52,910,914 TCF4
    nsv7010835copy number variation1nstd229human GRCh38 chr18: 55,515,327-55,515,539 , GRCh37.p13 chr18: 53,182,558-53,182,770 TCF4
    nsv7010779copy number variation1nstd229human GRCh38 chr18: 55,213,101-55,222,000 , GRCh37.p13 chr18: 52,880,332-52,889,231 TCF4
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