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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098778copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,827,722-73,835,910 , GRCh38.p12 chr17: 75,831,641-75,839,829 UNC13D
    nsv7094987copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,824,046-73,830,244 , GRCh38.p12 chr17: 75,827,965-75,834,163 UNC13D
    nsv7073965inversion1nstd229human GRCh38 chr17: 75,577,011-75,829,469 , GRCh37.p13 chr17: 73,573,092-73,825,550 UNK, SMIM5, 10 more genes
    nsv7062058inversion1nstd229human GRCh38 chr17: 75,576,996-75,829,470 , GRCh37.p13 chr17: 73,573,077-73,825,551 UNC13D, SMIM5, 10 more genes
    nsv6996812copy number variation1nstd229human GRCh38 chr17: 75,830,143-75,898,563 , GRCh37.p13 chr17: 73,826,224-73,894,644 WBP2, UNC13D, 3 more genes
    nsv6994008copy number variation1nstd229human GRCh38 chr17: 75,810,704-75,834,298 , GRCh37.p13 chr17: 73,806,785-73,830,379 UNC13D, UNK
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983209copy number variation1nstd229human GRCh38 chr17: 75,729,714-75,830,368 , GRCh37.p13 chr17: 73,725,795-73,826,449 UNC13D, MIR4738, 4 more genes
    nsv6980235copy number variation1nstd229human GRCh38 chr17: 75,829,002-75,831,876 , GRCh37.p13 chr17: 73,825,083-73,827,957 UNC13D
    nsv6979246copy number variation1nstd229human GRCh38 chr17: 75,833,301-75,837,300 , GRCh37.p13 chr17: 73,829,382-73,833,381 UNC13D
    nsv6589966inversion1nstd223human GRCh38 chr17: 75,576,986-75,829,587 , GRCh37.p13 chr17: 73,573,067-73,825,668 RECQL5, MIR4738, 10 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6201518copy number variation1nstd214human GRCh38 chr17: 75,832,813-75,832,902 , GRCh37.p13 chr17: 73,828,894-73,828,983 UNC13D
    nsv6082564insertion1nstd212human GRCh38 chr17: 75,825,545-75,825,545 , GRCh37.p13 chr17: 73,821,626-73,821,626 UNK, UNC13D
    nsv5869627copy number variation1nstd209human GRCh38 chr17: 75,844,028-75,845,096 , GRCh37.p13 chr17: 73,840,109-73,841,177 WBP2, UNC13D
    nsv5700257mobile element insertion1nstd211human GRCh38 chr17: 75,825,557-75,825,557 , GRCh37.p13 chr17: 73,821,638-73,821,638 UNC13D, UNK
    nsv5646828insertion1nstd207human GRCh38 chr17: 75,828,429-75,828,429 , GRCh37.p13 chr17: 73,824,510-73,824,510 UNC13D
    nsv5564314copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,824,026-73,826,583 , GRCh38.p12 chr17: 75,827,945-75,830,502 UNC13D
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