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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927890copy number variation1nstd209human GRCh38 chr16: 66,940,488-67,029,326 , GRCh37.p13 chr16: 66,974,391-67,063,229 CBFB, CES2, 4 more genes
    nsv5884944copy number variation1nstd209human GRCh38 chr16: 66,986,156-67,009,761 , GRCh37.p13 chr16: 67,020,059-67,043,664 CES4A
    nsv5723513mobile element insertion1nstd211human GRCh38 chr16: 67,010,059-67,010,059 , GRCh37.p13 chr16: 67,043,962-67,043,962 CES4A
    nsv5716550mobile element insertion1nstd211human GRCh38 chr16: 67,003,590-67,003,590 , GRCh37.p13 chr16: 67,037,493-67,037,493 CES4A
    nsv5558947mobile element insertion1nstd206human GRCh38 chr16: 67,003,602-67,003,641 , GRCh37.p13 chr16: 67,037,505-67,037,544 CES4A
    nsv5532815copy number variation1nstd206human GRCh38 chr16: 66,940,488-67,029,328 , GRCh37.p13 chr16: 66,974,391-67,063,231 CBFB, CES2, 4 more genes
    nsv5278114copy number variation1nstd204human GRCh38.p13 chr16: 66,988,481-66,991,759 , GRCh37.p13 chr16: 67,022,384-67,025,662 CES4A
    nsv5188298mobile element insertion1nstd203human GRCh38 chr16: 67,003,594-67,003,594 , GRCh37.p13 chr16: 67,037,497-67,037,497 CES4A
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005777copy number variation1nstd200human GRCh38 chr16: 66,940,488-67,029,328 , GRCh37.p13 chr16: 66,974,391-67,063,231 CES3, LOC107984881, 4 more genes
    nsv4993082copy number variation1nstd200human GRCh38 chr16: 67,004,431-67,005,938 , GRCh37.p13 chr16: 67,038,334-67,039,841 CES4A
    nsv4993081copy number variation1nstd200human GRCh38 chr16: 66,984,318-66,988,952 , GRCh37.p13 chr16: 67,018,221-67,022,855 CES4A
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4864202copy number variation1nstd200human GRCh37 chr16: 66,974,391-67,063,231 , GRCh38.p12 chr16: 66,940,488-67,029,328 CES3, CES4A, 4 more genes
    nsv4857459copy number variation1nstd200human GRCh37 chr16: 67,041,795-67,044,388 , GRCh38.p12 chr16: 67,007,892-67,010,485 CES4A
    nsv4760716insertion1nstd199human GRCh37 chr16: 67,037,502-67,037,502 , GRCh38.p12 chr16: 67,003,599-67,003,599 CES4A
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv4575464mobile element insertion1nstd166human GRCh37.p13 chr16: 67,037,493-67,037,493 , GRCh38.p12 chr16: 67,003,590-67,003,590 CES4A
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