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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095753copy number variation1nstd102humanPathogenic GRCh37 chr1: 153,782,653-153,964,569 , GRCh38.p12 chr1: 153,810,177-153,992,093 JTB, LOC101928059, 10 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
    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
    nsv6642457copy number variation1nstd229human GRCh38 chr1: 153,939,024-153,953,558 , GRCh37.p13 chr1: 153,911,500-153,926,034 DENND4B, CRTC2
    nsv6642437copy number variation1nstd229human GRCh38 chr1: 153,574,701-154,062,600 , GRCh37.p13 chr1: 153,547,177-154,035,076 S100A13, S100A16, 27 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6133926copy number variation1nstd213human GRCh37 chr1: 153,540,000-154,010,001 , GRCh38.p12 chr1: 153,567,524-154,037,525 SNAPIN, LOC645965, 26 more genes
    nsv6133737copy number variation1nstd213human GRCh37 chr1: 153,820,000-155,320,001 , GRCh38.p12 chr1: 153,847,524-155,350,210 GBA1LP, PKLR, 81 more genes
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133560copy number variation1nstd213human GRCh37 chr1: 153,460,000-155,250,001 , GRCh38.p12 chr1: 153,487,524-155,280,210 CKS1B, ILF2, 97 more genes
    nsv5422868copy number variation1nstd206human GRCh38 chr1: 153,931,759-153,932,070 , GRCh37.p13 chr1: 153,904,235-153,904,546 DENND4B, LOC101928059
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5285847copy number variation1nstd204human GRCh38.p13 chr1: 153,939,001-153,953,587 , GRCh37.p13 chr1: 153,911,477-153,926,063 DENND4B, CRTC2
    nsv5209109copy number variation1nstd204human GRCh38.p13 chr1: 153,938,801-153,953,500 , GRCh37.p13 chr1: 153,911,277-153,925,976 CRTC2, DENND4B
    nsv5207947copy number variation1nstd204human GRCh38.p13 chr1: 153,943,201-153,967,100 , GRCh37.p13 chr1: 153,915,677-153,939,576 DENND4B, SLC39A1, 3 more genes
    nsv5201886copy number variation1nstd204human GRCh38.p13 chr1: 153,939,113-153,953,416 , GRCh37.p13 chr1: 153,911,589-153,925,892 DENND4B, CRTC2
    nsv4903898copy number variation1nstd200human GRCh38 chr1: 153,891,283-154,169,965 , GRCh37.p13 chr1: 153,863,759-154,142,441 DENND4B, RN7SL431P, 15 more genes
    nsv4781208copy number variation1nstd200human GRCh37 chr1: 153,911,500-153,926,034 , GRCh38.p12 chr1: 153,939,024-153,953,558 DENND4B, CRTC2
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