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Items: 1 to 20 of 138

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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
    nsv7057328inversion1nstd229human GRCh38 chr1: 154,938,555-155,849,490 , GRCh37.p13 chr1: 154,911,031-155,819,281 ENTREP3, YY1AP1, 57 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
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv6642715copy number variation1nstd229human GRCh38 chr1: 155,135,292-155,165,181 , GRCh37.p13 chr1: 155,107,768-155,137,657 EFNA1, HMGN2P18, 2 more genes
    nsv6642714copy number variation1nstd229human GRCh38 chr1: 155,135,001-155,207,245 , GRCh37.p13 chr1: 155,107,477-155,177,036 MTX1, DPM3, 9 more genes
    nsv6332159copy number variation1nstd223human GRCh38 chr1: 155,080,703-155,146,082 , GRCh37.p13 chr1: 155,053,179-155,118,558 EFNA3, DPM3, 2 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
    nsv6310592copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,112,438-155,112,716 , GRCh38.p12 chr1: 155,139,962-155,140,240 DPM3
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6297100copy number variation1nstd186human GRCh37 chr1: 155,020,127-155,147,501 , GRCh38.p12 chr1: 155,047,651-155,175,025 ADAM15, DPM3, 9 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
    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
    nsv6133504copy number variation1nstd213human GRCh37 chr1: 154,420,000-155,500,001 , GRCh38.p12 chr1: 154,447,524-155,530,210 EFNA1, GBA1LP, 51 more genes
    nsv5423972copy number variation1nstd206human GRCh38 chr1: 155,047,651-155,175,025 , GRCh37.p13 chr1: 155,020,127-155,147,501 DCST1, EFNA4, 9 more genes
    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
    nsv5347270translocation1nstd200human GRCh38 chr7: 83,401,202-83,401,202 , GRCh38 chr1: 155,140,531-155,140,531 , GRCh37.p13 chr1: 155,113,007-155,113,007 , GRCh37.p13 chr7: 83,030,518-83,030,518 SEMA3E, DPM3
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