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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065329inversion1nstd229human GRCh38 chr17: 75,958,231-76,360,906 , GRCh37.p13 chr17: 73,954,312-74,356,987 RNF157, ACOX1, 20 more genes
    nsv6994257copy number variation1nstd229human GRCh38 chr17: 76,174,168-76,511,387 , GRCh37.p13 chr17: 74,170,249-74,507,469 RNF157, UBE2O, 12 more genes
    nsv6991247copy number variation1nstd229human GRCh38 chr17: 76,256,601-76,264,400 , GRCh37.p13 chr17: 74,252,682-74,260,481 LOC105371896, UBALD2
    nsv6987178copy number variation1nstd229human GRCh38 chr17: 76,254,701-76,269,000 , GRCh37.p13 chr17: 74,250,782-74,265,081 UBALD2, LOC105371896
    nsv6986426copy number variation1nstd229human GRCh38 chr17: 76,257,715-76,264,434 , GRCh37.p13 chr17: 74,253,796-74,260,515 LOC105371896, UBALD2
    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
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 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
    nsv6526975copy number variation1nstd223human GRCh38 chr17: 76,241,101-76,265,300 , GRCh37.p13 chr17: 74,237,182-74,261,381 LOC105371896, UBALD2
    nsv6515890copy number variation1nstd223human GRCh38 chr17: 76,257,715-76,264,431 , GRCh37.p13 chr17: 74,253,796-74,260,512 UBALD2, LOC105371896
    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
    nsv5701318mobile element insertion2nstd211human GRCh38 chr17: 76,269,894-76,269,894 , GRCh37.p13 chr17: 74,265,975-74,265,975 QRICH2, UBALD2
    nsv5533607copy number variation1nstd206human GRCh38 chr17: 76,268,596-76,274,419 , GRCh37.p13 chr17: 74,264,677-74,270,500 UBALD2, QRICH2
    nsv5514133copy number variation1nstd206human GRCh38 chr17: 76,257,715-76,264,431 , GRCh37.p13 chr17: 74,253,796-74,260,512 , UBALD2, 1 more genes
    nsv5422211mobile element insertion1nstd206human GRCh38 chr17: 76,269,894-76,269,945 , GRCh37.p13 chr17: 74,265,975-74,266,026 QRICH2, UBALD2
    nsv5349678translocation1nstd200human GRCh38 chr17: 76,264,431-76,264,431 , GRCh38 chr17: 76,257,714-76,257,714 , GRCh37.p13 chr17: 74,260,512-74,260,512 , GRCh37.p13 chr17: 74,253,795-74,253,795 LOC105371896, UBALD2
    nsv5331710translocation1nstd200human GRCh37 chr17: 74,253,796-74,253,796 , GRCh37 chr17: 74,260,512-74,260,512 , GRCh38.p12 chr17: 76,264,431-76,264,431 , GRCh38.p12 chr17: 76,257,715-76,257,715 LOC105371896, UBALD2
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv4680180copy number variation1nstd189human GRCh37.p13 chr17: 74,053,616-74,648,486 , GRCh38.p12 chr17: 76,057,535-76,652,404 , AANAT, 30 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
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