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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145925copy number variation1nstd232human GRCh37.p13 chr12: 133,046,236-133,046,396 , GRCh38.p12 chr12: 132,469,650-132,469,810 MUC8
    nsv7144937copy number variation1nstd232human GRCh37.p13 chr12: 133,049,680-133,049,799 , GRCh38.p12 chr12: 132,473,094-132,473,213 MUC8
    nsv7099028copy number variation1nstd102humanUncertain significance GRCh38 chr12: 132,237,283-132,491,257 , GRCh37.p13 chr12|NW_003315937.1: 11,322-165,247 , GRCh37.p13 chr12: 132,808,130-132,967,794 LOC105370092, LOC112268102, 5 more genes
    nsv7093960copy number variation1nstd102humanUncertain significance GRCh37 chr12: 132,414,268-133,263,901 , GRCh38.p12 chr12: 131,929,723-132,687,315 LOC107987169, NOC4L, 20 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7067298inversion1nstd229human GRCh38 chr12: 132,079,777-132,851,356 , GRCh37.p13 chr12: 132,564,322-133,427,942 LRCOL1, PGAM5, 26 more genes
    nsv6932192copy number variation1nstd229human GRCh38 chr12: 132,038,649-132,478,593 , GRCh37.p13 chr12: 132,523,194-133,055,179 EP400P1, LOC112268102, 11 more genes
    nsv6931261copy number variation1nstd229human GRCh38 chr12: 132,427,434-132,485,562 , GRCh37.p13 chr12: 133,004,020-133,062,148 LOC112268102, MUC8, 1 more genes
    nsv6931093copy number variation1nstd229human GRCh38 chr12: 132,476,138-132,476,236 , GRCh37.p13 chr12: 133,052,724-133,052,822 MUC8
    nsv6927656copy number variation1nstd229human GRCh38 chr12: 132,201,344-132,479,415 , GRCh37.p13 chr12|NW_003315937.1: 1-165,247 , GRCh37.p13 chr12: 132,685,889-133,056,001 GALNT9-AS1, MUC8, 5 more genes
    nsv6925477copy number variation1nstd229human GRCh38 chr12: 132,396,901-132,564,500 , GRCh37.p13 chr12: 132,973,487-133,141,086 LOC112268102, FBRSL1, 2 more genes
    nsv6922960copy number variation1nstd229human GRCh38 chr12: 132,436,083-132,469,609 , GRCh37.p13 chr12: 133,012,669-133,046,195 LOC112268102, MUC8, 1 more genes
    nsv6920492copy number variation1nstd229human GRCh38 chr12: 132,465,997-132,472,324 , GRCh37.p13 chr12: 133,042,583-133,048,910 MUC8
    nsv6621313copy number variation1nstd224human GRCh37 chr12: 133,041,618-133,069,894 , GRCh38.p12 chr12: 132,465,032-132,493,308 FBRSL1, MUC8
    nsv6479036copy number variation1nstd223human GRCh38 chr12: 132,476,624-132,480,777 , GRCh37.p13 chr12: 133,053,210-133,057,363 MUC8
    nsv6477898copy number variation1nstd223human GRCh38 chr12: 132,427,433-132,485,561 , GRCh37.p13 chr12: 133,004,019-133,062,147 LOC105370092, LOC112268102, 1 more genes
    nsv6314128copy number variation1nstd102humanUncertain significance GRCh37 chr12: 131,657,203-133,227,428 , GRCh38.p12 chr12: 131,172,658-132,650,842 RNA5SP377, LOC107987177, 42 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6274930copy number variation1nstd214human GRCh38 chr12: 132,469,760-132,469,828 , GRCh37.p13 chr12: 133,046,346-133,046,414 MUC8
    nsv6274772copy number variation1nstd214human GRCh38 chr12: 132,473,983-132,474,145 , GRCh37.p13 chr12: 133,050,569-133,050,731 MUC8
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