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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937759copy number variation1nstd209human GRCh38 chr18: 21,822,053-21,827,014 , GRCh37.p13 chr18: 19,402,014-19,406,975 MIR133A1, MIR1-2, 2 more genes
    nsv5872367copy number variation1nstd209human GRCh38 chr18: 21,822,078-21,826,789 , GRCh37.p13 chr18: 19,402,039-19,406,750 MIR133A1HG, MIB1, 1 more genes
    nsv5723079mobile element insertion1nstd211human GRCh38 chr18: 21,826,906-21,826,906 , GRCh37.p13 chr18: 19,406,867-19,406,867 MIR133A1HG, MIB1
    nsv5709873mobile element insertion1nstd211human GRCh38 chr18: 21,825,158-21,825,158 , GRCh37.p13 chr18: 19,405,119-19,405,119 MIB1, MIR133A1, 1 more genes
    nsv5422242mobile element insertion1nstd206human GRCh38 chr18: 21,825,158-21,825,209 , GRCh37.p13 chr18: 19,405,119-19,405,170 MIB1, MIR133A1, 1 more genes
    nsv5365810translocation1nstd200human GRCh38 chr18: 21,827,015-21,827,015 , GRCh38 chr18: 21,822,053-21,822,053 , GRCh37.p13 chr18: 19,402,014-19,402,014 , GRCh37.p13 chr18: 19,406,976-19,406,976 MIB1, MIR1-2, 1 more genes
    nsv5154671mobile element insertion1nstd203human GRCh38 chr18: 21,827,314-21,827,327 , GRCh37.p13 chr18: 19,407,275-19,407,288 MIB1, MIR1-2, 1 more genes
    nsv5026866copy number variation1nstd200human GRCh38 chr18: 21,653,980-21,877,770 , GRCh37.p13 chr18: 19,233,941-19,457,731 , MIB1, 7 more genes
    nsv4854580copy number variation1nstd200human GRCh37 chr18: 19,402,014-19,406,976 , GRCh38.p12 chr18: 21,822,053-21,827,015 MIB1, MIR133A1, 2 more genes
    nsv4630265copy number variation1nstd183human GRCh37 chr18: 19,339,825-19,481,950 , GRCh38.p12 chr18: 21,759,864-21,901,989 MIB1, MIR1-2, 6 more genes
    nsv4561189mobile element insertion1nstd166human GRCh37.p13 chr18: 19,404,875-19,404,875 , GRCh38.p12 chr18: 21,824,914-21,824,914 MIB1, MIR133A1, 1 more genes
    nsv4505268mobile element insertion1nstd166human GRCh37.p13 chr18: 19,407,275-19,407,275 , GRCh38.p12 chr18: 21,827,314-21,827,314 MIB1, MIR1-2, 1 more genes
    nsv4457415copy number variation1nstd102humanUncertain significance GRCh37 chr18: 19,047,402-19,737,070 , GRCh38.p12 chr18: 21,467,441-22,157,109 ABHD3, RPL34P32, 15 more genes
    nsv4271360copy number variation1nstd166human GRCh37.p13 chr18: 19,402,028-19,406,976 , GRCh38.p12 chr18: 21,822,067-21,827,015 MIR133A1HG, MIR1-2, 2 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
    nsv3923838copy number variation1nstd102humanPathogenic NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381 WDR7-OT1, HMGN1P30, 941 more genes
    nsv3921458copy number variation1nstd102humanPathogenic NCBI36 chr18: 13,330,111-19,243,841 , GRCh37 chr18: 13,340,111-20,989,843 , GRCh38 chr18: 13,340,112-23,409,879 TERF1P2, RPL34P32, 97 more genes
    nsv3920818copy number variation1nstd102humanPathogenic NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298 AQP4-AS1, SERPINB8, 670 more genes
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