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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5529882copy number variation1nstd206human GRCh38 chr15: 88,475,544-88,482,191 , GRCh37.p13 chr15: 89,018,775-89,025,422 MRPS11
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5009144copy number variation1nstd200human GRCh38 chr15: 88,475,545-88,482,191 , GRCh37.p13 chr15: 89,018,776-89,025,422 MRPS11
    nsv5002247copy number variation1nstd200human GRCh38 chr15: 88,468,985-88,470,246 , GRCh37.p13 chr15: 89,012,216-89,013,477 MRPS11
    nsv4863943copy number variation1nstd200human GRCh37 chr15: 89,018,774-89,025,423 , GRCh38.p12 chr15: 88,475,543-88,482,192 MRPS11
    nsv4856230copy number variation1nstd200human GRCh37 chr15: 89,012,216-89,013,477 , GRCh38.p12 chr15: 88,468,985-88,470,246 MRPS11
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4575006mobile element insertion1nstd166human GRCh37.p13 chr15: 89,023,457-89,023,457 , GRCh38.p12 chr15: 88,480,226-88,480,226 MRPS11
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4250878copy number variation1nstd166human GRCh37.p13 chr15: 89,018,838-89,025,422 , GRCh38.p12 chr15: 88,475,607-88,482,191 MRPS11
    nsv4250556copy number variation1nstd166human GRCh37.p13 chr15: 88,660,820-89,014,484 , GRCh38.p12 chr15: 88,117,589-88,471,253 NTRK3, MRPL46, 6 more genes
    nsv3924544copy number variation1nstd102humanUncertain significance NCBI36 chr15: 86,443,734-86,819,080 , GRCh37.p13 chr15: 88,642,730-89,018,076 , GRCh38.p12 chr15: 88,099,499-88,474,845 MRPL46, MED28P6, 6 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919393copy number variation1nstd102humanPathogenic NCBI36 chr15: 84,170,900-100,278,724 , GRCh37 chr15: 86,369,896-102,461,201 , GRCh38 chr15: 85,826,665-101,920,998 LOC105370997, LOC102724465, 270 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
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