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Items: 1 to 20 of 381

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145845insertion1nstd232human GRCh37.p13 chr4: 115,549,930-115,549,930 , GRCh38.p12 chr4: 114,628,774-114,628,774 UGT8
    nsv7056396inversion1nstd229human GRCh38 chr4: 114,596,236-114,598,835 , GRCh37.p13 chr4: 115,517,392-115,519,991 UGT8
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv7044361inversion1nstd229human GRCh38 chr4: 114,587,963-114,599,280 , GRCh37.p13 chr4: 115,509,119-115,520,436 UGT8
    nsv7039674inversion1nstd229human GRCh38 chr4: 114,614,990-114,615,053 , GRCh37.p13 chr4: 115,536,146-115,536,209 UGT8
    nsv6757052copy number variation1nstd229human GRCh38 chr4: 114,623,166-114,948,851 , GRCh37.p13 chr4: 115,544,322-115,870,007 NDST4, MIR577, 4 more genes
    nsv6756890copy number variation1nstd229human GRCh38 chr4: 114,611,696-114,611,920 , GRCh37.p13 chr4: 115,532,852-115,533,076 UGT8
    nsv6756320copy number variation1nstd229human GRCh38 chr4: 114,640,992-114,641,113 , GRCh37.p13 chr4: 115,562,148-115,562,269 UGT8
    nsv6755439copy number variation1nstd229human GRCh38 chr4: 114,646,076-114,648,900 , GRCh37.p13 chr4: 115,567,232-115,570,056 UGT8
    nsv6755024copy number variation1nstd229human GRCh38 chr4: 114,673,995-114,700,360 , GRCh37.p13 chr4: 115,595,151-115,621,516 UGT8
    nsv6754781copy number variation1nstd229human GRCh38 chr4: 114,621,154-114,621,611 , GRCh37.p13 chr4: 115,542,310-115,542,767 UGT8
    nsv6753323copy number variation1nstd229human GRCh38 chr4: 114,678,587-114,692,679 , GRCh37.p13 chr4: 115,599,743-115,613,835 UGT8
    nsv6752670copy number variation1nstd229human GRCh38 chr4: 114,597,404-114,597,528 , GRCh37.p13 chr4: 115,518,560-115,518,684 UGT8
    nsv6749004copy number variation1nstd229human GRCh38 chr4: 114,686,883-114,689,824 , GRCh37.p13 chr4: 115,608,039-115,610,980 UGT8
    nsv6747688copy number variation1nstd229human GRCh38 chr4: 114,599,592-114,610,682 , GRCh37.p13 chr4: 115,520,748-115,531,838 UGT8
    nsv6746060copy number variation1nstd229human GRCh38 chr4: 114,603,191-114,609,050 , GRCh37.p13 chr4: 115,524,347-115,530,206 UGT8
    nsv6745901copy number variation1nstd229human GRCh38 chr4: 114,628,535-114,628,892 , GRCh37.p13 chr4: 115,549,691-115,550,048 UGT8
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6395368copy number variation1nstd223human GRCh38 chr4: 114,687,735-114,688,392 , GRCh37.p13 chr4: 115,608,891-115,609,548 UGT8
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