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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949513insertion1nstd209human GRCh38 chr6: 13,925,069-13,925,069 , GRCh37.p13 chr6: 13,925,300-13,925,300 RNF182
    nsv5684668mobile element insertion1nstd211human GRCh38 chr6: 13,949,836-13,949,836 , GRCh37.p13 chr6: 13,950,067-13,950,067 MRPL35P1, RNF182
    nsv5626461insertion1nstd207human GRCh38 chr6: 13,925,069-13,925,069 , GRCh37.p13 chr6: 13,925,300-13,925,300 RNF182
    nsv5413270mobile element insertion1nstd206human GRCh38 chr6: 13,949,836-13,949,887 , GRCh37.p13 chr6: 13,950,067-13,950,118 MRPL35P1, RNF182
    nsv5369242translocation1nstd200human GRCh38 chr6: 13,953,918-13,953,918 , GRCh38 chr6: 13,956,496-13,956,496 , GRCh37.p13 chr6: 13,954,149-13,954,149 , GRCh37.p13 chr6: 13,956,727-13,956,727 RNF182
    nsv5090706mobile element insertion1nstd203human GRCh38 chr6: 13,923,190-13,923,204 , GRCh37.p13 chr6: 13,923,421-13,923,435 RNF182
    nsv4934436copy number variation1nstd200human GRCh38 chr6: 13,970,580-14,047,459 , GRCh37.p13 chr6: 13,970,811-14,047,690 RNF182
    nsv4932786copy number variation1nstd200human GRCh38 chr6: 13,925,802-13,926,292 , GRCh37.p13 chr6: 13,926,033-13,926,523 RNF182
    nsv4932783copy number variation1nstd200human GRCh38 chr6: 13,876,370-14,003,982 , GRCh37.p13 chr6: 13,876,601-14,004,213 RNF182, MRPL35P1
    nsv4828505copy number variation1nstd200human GRCh37 chr6: 13,970,811-14,047,690 , GRCh38.p12 chr6: 13,970,580-14,047,459 RNF182
    nsv4751489insertion1nstd199human GRCh37 chr6: 13,925,293-13,925,293 , GRCh38.p12 chr6: 13,925,062-13,925,062 RNF182
    nsv4598382copy number variation1nstd183human GRCh37 chr6: 13,925,064-13,925,264 , GRCh38.p12 chr6: 13,924,833-13,925,033 RNF182
    nsv4539598insertion1nstd166human GRCh37.p13 chr6: 13,957,371-13,957,371 , GRCh38.p12 chr6: 13,957,140-13,957,140 RNF182
    nsv4490106mobile element insertion1nstd166human GRCh37.p13 chr6: 13,961,148-13,961,148 , GRCh38.p12 chr6: 13,960,917-13,960,917 RNF182
    nsv4478572mobile element insertion1nstd166human GRCh37.p13 chr6: 13,950,051-13,950,051 , GRCh38.p12 chr6: 13,949,820-13,949,820 MRPL35P1, RNF182
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456299copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975 LOC101928354, MBOAT1, 101 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv4455886copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,933,934-14,154,068 , GRCh38.p12 chr6: 13,933,703-14,153,837 MRPL35P1, LOC105374939, 2 more genes
    nsv4439487insertion1nstd175human GRCh37 chr6: 13,925,300-13,925,300 , GRCh38.p12 chr6: 13,925,069-13,925,069 RNF182
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