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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929051copy number variation1nstd209human GRCh38 chr15: 89,325,034-89,325,231 , GRCh37.p13 chr15: 89,868,265-89,868,462 MIR6766, POLG
    nsv5672828copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,790,873-89,876,991 , GRCh38.p12 chr15: 89,247,642-89,333,760 POLG, TRR-TCG1-1, 2 more genes
    nsv5663654insertion1nstd207human GRCh38 chr15: 89,325,195-89,325,195 , GRCh37.p13 chr15: 89,868,426-89,868,426 MIR6766, POLG
    nsv5659584insertion1nstd207human GRCh38 chr15: 89,325,073-89,325,073 , GRCh37.p13 chr15: 89,868,304-89,868,304 POLG, MIR6766
    nsv5656917insertion1nstd207human GRCh38 chr15: 89,325,273-89,325,273 , GRCh37.p13 chr15: 89,868,504-89,868,504 MIR6766, POLG
    nsv5597244copy number variation1nstd207human GRCh38 chr15: 89,325,041-89,325,110 , GRCh37.p13 chr15: 89,868,272-89,868,341 POLG, MIR6766
    nsv5588393copy number variation1nstd207human GRCh38 chr15: 89,325,087-89,325,270 , GRCh37.p13 chr15: 89,868,318-89,868,501 POLG, MIR6766
    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
    nsv5300841copy number variation1nstd204human GRCh37.p13 chr15: 89,868,257-89,868,511 , GRCh38.p13 chr15: 89,325,026-89,325,280 POLG, MIR6766
    nsv4732649copy number variation1nstd199human GRCh37 chr15: 89,868,283-89,868,476 , GRCh38.p12 chr15: 89,325,052-89,325,245 POLG, MIR6766
    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
    nsv4675189copy number variation1nstd102humanUncertain significance GRCh37 chr15: 89,669,751-89,899,031 , GRCh38.p12 chr15: 89,126,520-89,355,800 FANCI, MIR6766, 5 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
    nsv4650693copy number variation1nstd186human GRCh37 chr15: 89,868,315-89,868,577 , GRCh38.p12 chr15: 89,325,084-89,325,346 POLG, MIR6766
    nsv4626753copy number variation1nstd183human GRCh37 chr15: 89,684,517-90,163,339 , GRCh38.p12 chr15: 89,141,286-89,620,108 , ABHD2, 14 more genes
    nsv4456267copy number variation1nstd102humanUncertain significance GRCh37 chr15: 89,828,317-89,874,912 , GRCh38.p12 chr15: 89,285,086-89,331,681 MIR6766, POLG, 1 more genes
    nsv4447107insertion1nstd175human GRCh37 chr15: 89,868,366-89,868,366 , GRCh38.p12 chr15: 89,325,135-89,325,135 POLG, MIR6766
    nsv4415443copy number variation1nstd174human GRCh37 chr15: 89,868,307-89,868,505 , GRCh38.p12 chr15: 89,325,076-89,325,274 MIR6766, POLG
    nsv4414855copy number variation1nstd174human GRCh37 chr15: 89,868,132-89,868,604 , GRCh38.p12 chr15: 89,324,901-89,325,373 MIR6766, POLG
    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
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