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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5921920copy number variation1nstd209human GRCh38 chr12: 3,058,695-6,171,259 , GRCh37.p13 chr12: 3,167,861-6,280,425 , LOC105369623, 54 more genes
    nsv5649491insertion1nstd207human GRCh38 chr12: 4,545,440-4,545,440 , GRCh37.p13 chr12: 4,654,606-4,654,606 RAD51AP1
    nsv5499136copy number variation1nstd206human GRCh38 chr12: 4,548,178-4,548,684 , GRCh37.p13 chr12: 4,657,344-4,657,850 RAD51AP1
    nsv5381764copy number variation1nstd102humanPathogenic GRCh37 chr12: 3,619,010-5,221,363 , GRCh38.p12 chr12: 3,509,844-5,112,197 OTUD4P1, LOC105369612, 30 more genes
    nsv5380741copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,479,509-6,235,003 , GRCh38.p12 chr12: 4,370,343-6,125,837 ANO2, LOC105369617, 25 more genes
    nsv5135196mobile element insertion1nstd203human GRCh38 chr12: 4,540,891-4,540,904 , GRCh37.p13 chr12: 4,650,057-4,650,070 RAD51AP1
    nsv4971934copy number variation1nstd200human GRCh38 chr12: 4,549,506-4,550,170 , GRCh37.p13 chr12: 4,658,672-4,659,336 RAD51AP1
    nsv4833224copy number variation1nstd200human GRCh37 chr12: 4,658,672-4,659,336 , GRCh38.p12 chr12: 4,549,506-4,550,170 RAD51AP1
    nsv4729176copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,242-4,683,495 , GRCh38.p12 chr12: 82,076-4,574,329 RPL18P9, CACNA1C, 92 more genes
    nsv4713062copy number variation1nstd195human GRCh37 chr12: 4,660,316-4,660,317 , GRCh38.p12 chr12: 4,551,150-4,551,151 RAD51AP1
    nsv4679795copy number variation1nstd189human GRCh37.p13 chr12: 4,504,235-4,966,214 , GRCh38.p12 chr12: 4,395,069-4,857,048 , FGF6, 10 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4608860copy number variation1nstd183human GRCh37 chr12: 4,668,321-4,669,173 , GRCh38.p12 chr12: 4,559,155-4,560,007 RAD51AP1
    nsv4457052copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926 TSPAN9, RNU6-174P, 118 more genes
    nsv4455658copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-8,393,815 , GRCh38.p12 chr12: 64,620-8,241,219 PLEKHG6, MIR141, 226 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4350818copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,216-15,001,420 , GRCh38.p12 chr12: 80,050-14,848,486 LOC107984495, KLRC1, 432 more genes
    nsv4349513copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,216-8,185,497 , GRCh38.p12 chr12: 80,050-8,032,901 LOC105369617, LRTM2, 214 more genes
    nsv4348793copy number variation1nstd102humanPathogenic GRCh37 chr12: 237,588-8,278,292 , GRCh38.p12 chr12: 128,422-8,125,696 RN7SL69P, GAPDH-DT, 216 more genes
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