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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099235copy number variation1nstd231human GRCh38.p12 chr1: 154,116,919-155,715,830 , GRCh37 chr1: 154,089,395-155,685,621 ADAR, CHRNB2, 80 more genes
    nsv7095703copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,420,581-154,422,476 , GRCh38.p12 chr1: 154,448,105-154,450,000 IL6R
    nsv7095320copy number variation1nstd102humanPathogenic GRCh37 chr1: 153,963,273-154,580,482 , GRCh38.p12 chr1: 153,990,797-154,608,006 RNU6-239P, ATP8B2, 30 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7044026inversion1nstd229human GRCh38 chr1: 154,465,327-154,467,269 , GRCh37.p13 chr1: 154,437,803-154,439,745 SHE, IL6R
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv7041246inversion1nstd229human GRCh38 chr1: 153,232,460-155,277,038 , GRCh37.p13 chr1: 153,204,936-155,246,829 INTS3, GBA1LP, 111 more genes
    nsv6642701copy number variation1nstd229human GRCh38 chr1: 154,459,063-154,462,912 , GRCh37.p13 chr1: 154,431,539-154,435,388 IL6R
    nsv6642700copy number variation1nstd229human GRCh38 chr1: 154,450,251-154,452,773 , GRCh37.p13 chr1: 154,422,727-154,425,249 IL6R
    nsv6642699copy number variation1nstd229human GRCh38 chr1: 154,439,040-154,443,397 , GRCh37.p13 chr1: 154,411,516-154,415,873 IL6R
    nsv6642698copy number variation1nstd229human GRCh38 chr1: 154,432,978-154,436,039 , GRCh37.p13 chr1: 154,405,454-154,408,515 IL6R
    nsv6642697copy number variation1nstd229human GRCh38 chr1: 154,406,208-154,416,796 , GRCh37.p13 chr1: 154,378,684-154,389,272 PSMD8P1, IL6R-AS1, 1 more genes
    nsv6642481copy number variation1nstd229human GRCh38 chr1: 154,423,745-154,424,111 , GRCh37.p13 chr1: 154,396,221-154,396,587 IL6R
    nsv6642352copy number variation1nstd229human GRCh38 chr1: 154,467,033-154,467,124 , GRCh37.p13 chr1: 154,439,509-154,439,600 SHE, IL6R
    nsv6642351copy number variation1nstd229human GRCh38 chr1: 154,447,079-154,452,576 , GRCh37.p13 chr1: 154,419,555-154,425,052 IL6R
    nsv6642246copy number variation1nstd229human GRCh38 chr1: 154,420,956-154,423,287 , GRCh37.p13 chr1: 154,393,432-154,395,763 IL6R
    nsv6635920copy number variation1nstd227human GRCh38.p12 chr1: 154,398,462-154,405,422 , GRCh37 chr1: 154,370,938-154,377,898 IL6R, IL6R-AS1
    nsv6332009copy number variation1nstd223human GRCh38 chr1: 154,449,989-154,453,030 , GRCh37.p13 chr1: 154,422,465-154,425,506 IL6R
    nsv6310727copy number variation1nstd102humanPathogenic GRCh37 chr1: 154,422,067-154,580,482 , GRCh38.p12 chr1: 154,449,591-154,608,006 ADAR, CHRNB2, 6 more genes
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