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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
    nsv7067018inversion1nstd229human GRCh38 chr14: 20,775,660-20,981,672 , GRCh37.p13 chr14: 21,243,819-21,449,831 LOC100507513, LOC100130571, 8 more genes
    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
    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
    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
    nsv6635271copy number variation1nstd227human GRCh38.p12 chr14: 20,889,996-20,937,726 , GRCh37 chr14: 21,358,155-21,405,885 RNASE3, RNASE2CP, 1 more genes
    nsv6622493copy number variation1nstd224human GRCh37 chr14: 21,343,164-21,422,666 , GRCh38.p12 chr14: 20,875,005-20,954,507 RNASE2, RNASE2CP, 2 more genes
    nsv6622492copy number variation2nstd224human GRCh37 chr14: 21,343,164-21,393,289 , GRCh38.p12 chr14: 20,875,005-20,925,130 RNASE2CP, RNASE3, 1 more genes
    nsv6622463copy number variation3nstd224human GRCh37 chr14: 21,360,216-21,393,289 , GRCh38.p12 chr14: 20,892,057-20,925,130 RNASE2CP, RNASE3, 1 more genes
    nsv6622462copy number variation1nstd224human GRCh37 chr14: 21,360,156-21,393,289 , GRCh38.p12 chr14: 20,891,997-20,925,130 RNASE2CP, RNASE3, 1 more genes
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