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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7076675inversion1nstd229human GRCh38 chr14: 20,783,342-20,981,448 , GRCh37.p13 chr14: 21,251,501-21,449,607 RNASE1, RNASE2, 7 more genes
    nsv7075961inversion1nstd229human GRCh38 chr14: 20,877,938-20,905,385 , GRCh37.p13 chr14: 21,346,097-21,373,544 LOC100507513, RNASE3
    nsv7067018inversion1nstd229human GRCh38 chr14: 20,775,660-20,981,672 , GRCh37.p13 chr14: 21,243,819-21,449,831 LOC100507513, LOC100130571, 8 more genes
    nsv7064330inversion1nstd229human GRCh38 chr14: 20,926,771-20,933,201 , GRCh37.p13 chr14: 21,394,930-21,401,360 LOC100507513
    nsv6957853copy number variation1nstd229human GRCh38 chr14: 20,881,901-20,953,800 , GRCh37.p13 chr14: 21,350,060-21,421,959 RNASE2CP, RNASE2, 2 more genes
    nsv6957216copy number variation1nstd229human GRCh38 chr14: 20,881,101-20,954,000 , GRCh37.p13 chr14: 21,349,260-21,422,159 LOC100507513, RNASE2CP, 2 more genes
    nsv6955873copy number variation1nstd229human GRCh38 chr14: 20,888,801-20,953,600 , GRCh37.p13 chr14: 21,356,960-21,421,759 RNASE2CP, RNASE2, 2 more genes
    nsv6955267copy number variation1nstd229human GRCh38 chr14: 20,886,986-20,892,168 , GRCh37.p13 chr14: 21,355,145-21,360,327 LOC100507513, RNASE3
    nsv6954650copy number variation1nstd229human GRCh38 chr14: 20,880,401-20,953,700 , GRCh37.p13 chr14: 21,348,560-21,421,859 RNASE2CP, RNASE2, 2 more genes
    nsv6953996copy number variation1nstd229human GRCh38 chr14: 20,889,601-20,953,600 , GRCh37.p13 chr14: 21,357,760-21,421,759 RNASE3, LOC100507513, 2 more genes
    nsv6952454copy number variation1nstd229human GRCh38 chr14: 20,885,301-20,954,000 , GRCh37.p13 chr14: 21,353,460-21,422,159 RNASE2CP, RNASE2, 2 more genes
    nsv6951393copy number variation1nstd229human GRCh38 chr14: 20,889,701-20,955,100 , GRCh37.p13 chr14: 21,357,860-21,423,259 RNASE3, RNASE2, 2 more genes
    nsv6947335copy number variation1nstd229human GRCh38 chr14: 20,881,701-20,953,900 , GRCh37.p13 chr14: 21,349,860-21,422,059 RNASE2, RNASE2CP, 2 more genes
    nsv6946540copy number variation1nstd229human GRCh38 chr14: 20,909,142-20,911,372 , GRCh37.p13 chr14: 21,377,301-21,379,531 LOC100507513
    nsv6940928copy number variation1nstd229human GRCh38 chr14: 20,874,292-20,878,958 , GRCh37.p13 chr14: 21,342,451-21,347,117 LOC100507513
    nsv6938921copy number variation1nstd229human GRCh38 chr14: 20,919,094-20,919,714 , GRCh37.p13 chr14: 21,387,253-21,387,873 RNASE2CP, LOC100507513
    nsv6938507copy number variation1nstd229human GRCh38 chr14: 20,882,301-20,953,700 , GRCh37.p13 chr14: 21,350,460-21,421,859 LOC100507513, RNASE2CP, 2 more genes
    nsv6637326copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,349,608-21,618,292 , GRCh38.p12 chr14: 20,881,449-21,150,133 RNASE13, ARHGEF40, 21 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
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