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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6748895copy number variation1nstd229human GRCh38 chr4: 67,544,201-67,570,900 , GRCh37.p13 chr4: 68,409,919-68,436,618 CENPC, STAP1
    nsv6738666copy number variation1nstd229human GRCh38 chr4: 66,318,664-67,575,458 , GRCh37.p13 chr4: 67,184,382-68,441,176 STAP1, RNU6-699P, 6 more genes
    nsv6637038copy number variation1nstd102humanUncertain significance GRCh37 chr4: 67,729,321-68,949,586 , GRCh38.p12 chr4: 66,863,603-68,083,868 UBA6-DT, LOC101927237, 24 more genes
    nsv6636883copy number variation1nstd102humanUncertain significance GRCh37 chr4: 66,215,872-68,647,080 , GRCh38.p12 chr4: 65,350,154-67,781,362 LOC100419046, LOC105377260, 24 more genes
    nsv6629940copy number variation1nstd224human GRCh37 chr4: 68,453,189-68,704,036 , GRCh38.p12 chr4: 67,587,471-67,838,318 TMPRSS11CP, LOC107986207, 9 more genes
    nsv6393167copy number variation1nstd223human GRCh38 chr4: 67,573,801-67,574,500 , GRCh37.p13 chr4: 68,439,519-68,440,218 STAP1
    nsv6384458copy number variation1nstd223human GRCh38 chr4: 67,580,109-67,587,975 , GRCh37.p13 chr4: 68,445,827-68,453,693 STAP1
    nsv6313845copy number variation1nstd102humanUncertain significance GRCh37 chr4: 68,272,006-68,923,410 , GRCh38.p12 chr4: 67,406,288-68,057,692 TMPRSS11F, TMPRSS11D, 20 more genes
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135600copy number variation1nstd213human GRCh37 chr4: 68,260,000-69,150,001 , GRCh38.p12 chr4: 67,394,282-68,284,283 TMPRSS11B, TMPRSS11BNL, 25 more genes
    nsv5997866copy number variation1nstd212human GRCh38 chr4: 67,561,967-67,562,237 , GRCh37.p13 chr4: 68,427,685-68,427,955 STAP1
    nsv5715526mobile element insertion2nstd211human GRCh38 chr4: 67,594,504-67,594,504 , GRCh37.p13 chr4: 68,460,222-68,460,222 STAP1
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5467993copy number variation1nstd206human GRCh38 chr4: 67,588,007-67,588,661 , GRCh37.p13 chr4: 68,453,725-68,454,379 STAP1
    nsv5179362mobile element insertion1nstd203human GRCh38 chr4: 67,594,486-67,594,504 , GRCh37.p13 chr4: 68,460,204-68,460,222 STAP1
    nsv5161395mobile element insertion1nstd203human GRCh38 chr4: 67,594,487-67,594,504 , GRCh37.p13 chr4: 68,460,205-68,460,222 STAP1
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925742copy number variation1nstd200human GRCh38 chr4: 67,580,002-67,588,100 , GRCh37.p13 chr4: 68,445,720-68,453,818 STAP1
    nsv4922767copy number variation1nstd200human GRCh38 chr4: 67,572,743-67,581,622 , GRCh37.p13 chr4: 68,438,461-68,447,340 STAP1
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