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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976038insertion1nstd209human GRCh38 chr13: 49,293,883-49,293,883 , GRCh37.p13 chr13: 49,868,019-49,868,019 CDADC1
    nsv5941198copy number variation1nstd209human GRCh38 chr13: 49,269,240-49,269,305 , GRCh37.p13 chr13: 49,843,376-49,843,441 CDADC1
    nsv5727173mobile element insertion1nstd211human GRCh38 chr13: 49,250,660-49,250,660 , GRCh37.p13 chr13: 49,824,796-49,824,796 CDADC1
    nsv5597599copy number variation1nstd207human GRCh38 chr13: 49,269,240-49,269,305 , GRCh37.p13 chr13: 49,843,376-49,843,441 CDADC1
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561330sequence alteration1nstd206human GRCh38 chr13: 44,983,377-49,709,767 , GRCh37.p13 chr13: 45,557,512-50,283,903 , ESD, 103 more genes
    nsv5497696copy number variation1nstd206human GRCh38 chr13: 49,256,147-49,257,488 , GRCh37.p13 chr13: 49,830,283-49,831,624 CDADC1
    nsv5495286copy number variation1nstd206human GRCh38 chr13: 49,257,728-49,257,823 , GRCh37.p13 chr13: 49,831,864-49,831,959 CDADC1
    nsv5307050copy number variation1nstd204human GRCh38.p13 chr13: 49,201,982-51,085,310 , GRCh37.p13 chr13: 49,776,118-51,659,446 , MLNR, 40 more genes
    nsv5265064copy number variation1nstd204human GRCh38.p13 chr13: 49,247,886-49,252,620 , GRCh37.p13 chr13: 49,822,022-49,826,756 LOC105370203, CDADC1
    nsv5263239copy number variation1nstd204human GRCh38.p13 chr13: 49,290,106-49,291,705 , GRCh37.p13 chr13: 49,864,242-49,865,841 CDADC1
    nsv5158967mobile element insertion1nstd203human GRCh38 chr13: 49,282,255-49,282,295 , GRCh37.p13 chr13: 49,856,391-49,856,431 CDADC1
    nsv5140803mobile element insertion1nstd203human GRCh38 chr13: 49,293,889-49,293,906 , GRCh37.p13 chr13: 49,868,025-49,868,042 CDADC1
    nsv4997414copy number variation1nstd200human GRCh38 chr13: 49,268,295-49,271,210 , GRCh37.p13 chr13: 49,842,431-49,845,346 CDADC1
    nsv4997413copy number variation1nstd200human GRCh38 chr13: 49,228,530-49,247,755 , GRCh37.p13 chr13: 49,802,666-49,821,891 THAP12P10, CDADC1, 1 more genes
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4846866copy number variation1nstd200human GRCh37 chr13: 49,802,666-49,821,891 , GRCh38.p12 chr13: 49,228,530-49,247,755 THAP12P10, CDADC1, 1 more genes
    nsv4845274copy number variation1nstd200human GRCh37 chr13: 49,776,128-51,659,444 , GRCh38.p12 chr13: 49,201,992-51,085,308 , PHF11, 40 more genes
    nsv4830693copy number variation1nstd200human GRCh37 chr13: 49,842,431-49,845,346 , GRCh38.p12 chr13: 49,268,295-49,271,210 CDADC1
    nsv4737277copy number variation1nstd199human GRCh37 chr13: 49,849,852-49,849,920 , GRCh38.p12 chr13: 49,275,716-49,275,784 CDADC1
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