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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144610insertion1nstd232human GRCh38.p12 chr8: 66,922,727-66,922,727 , GRCh37.p13 chr8: 67,834,962-67,834,962 MCMDC2, SNHG6, 1 more genes
    nsv7061112inversion1nstd229human GRCh38 chr8: 66,903,922-66,903,951 , GRCh37.p13 chr8: 67,816,157-67,816,186 MCMDC2
    nsv7060811inversion1nstd229human GRCh38 chr8: 66,867,173-66,996,888 , GRCh37.p13 chr8: 67,779,408-67,909,123 PPP1R42, SNHG6, 4 more genes
    nsv6857951copy number variation1nstd229human GRCh38 chr8: 66,902,127-66,902,212 , GRCh37.p13 chr8: 67,814,362-67,814,447 MCMDC2
    nsv6856577copy number variation1nstd229human GRCh38 chr8: 66,880,799-66,880,978 , GRCh37.p13 chr8: 67,793,034-67,793,213 MCMDC2
    nsv6848593copy number variation1nstd229human GRCh38 chr8: 66,853,627-67,142,119 , GRCh37.p13 chr8: 67,765,862-68,054,354 SNHG6, C8orf44-SGK3, 10 more genes
    nsv6841307copy number variation1nstd229human GRCh38 chr8: 66,894,989-66,895,154 , GRCh37.p13 chr8: 67,807,224-67,807,389 MCMDC2
    nsv6841129copy number variation1nstd229human GRCh38 chr8: 66,886,327-66,890,251 , GRCh37.p13 chr8: 67,798,562-67,802,486 MCMDC2
    nsv6636616copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,642,641-68,406,704 , GRCh38.p12 chr8: 66,730,406-67,494,469 C8orf44-SGK3, LOC105375885, 16 more genes
    nsv6636205copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,261,729-68,676,568 , GRCh38.p12 chr8: 66,349,494-67,764,333 C8orf44-SGK3, SNHG6, 36 more genes
    nsv6633097copy number variation2nstd224human GRCh37 chr8: 67,786,385-67,817,462 , GRCh38.p12 chr8: 66,874,150-66,905,227 MCMDC2
    nsv6633020copy number variation1nstd224human GRCh37 chr8: 67,734,618-68,102,996 , GRCh38.p12 chr8: 66,822,383-67,190,761 MCMDC2, TCF24, 12 more genes
    nsv6632899copy number variation1nstd224human GRCh37 chr8: 67,786,385-68,163,686 , GRCh38.p12 chr8: 66,874,150-67,251,451 COPS5, SNHG6, 10 more genes
    nsv6568810inversion1nstd223human GRCh38 chr8: 66,881,682-66,882,485 , GRCh37.p13 chr8: 67,793,917-67,794,720 MCMDC2
    nsv6568428inversion1nstd223human GRCh38 chr8: 66,886,215-66,886,734 , GRCh37.p13 chr8: 67,798,450-67,798,969 MCMDC2
    nsv6567847inversion1nstd223human GRCh38 chr8: 66,899,629-66,899,921 , GRCh37.p13 chr8: 67,811,864-67,812,156 MCMDC2
    nsv6564738inversion1nstd223human GRCh38 chr8: 66,889,526-66,890,099 , GRCh37.p13 chr8: 67,801,761-67,802,334 MCMDC2
    nsv6424371copy number variation1nstd223human GRCh38 chr8: 66,791,690-67,039,259 , GRCh37.p13 chr8: 67,703,925-67,951,494 PPP1R42, LOC100288001, 7 more genes
    nsv6291302copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,676,966-67,792,479 , GRCh38.p12 chr8: 66,764,731-66,880,244 PTTG3P, MCMDC2, 2 more genes
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 LINC00967, LOC107986950, 64 more genes
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