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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721402mobile element insertion2nstd211human GRCh38 chr16: 30,552,407-30,552,407 , GRCh37.p13 chr16: 30,563,728-30,563,728 ZNF764
    nsv5520109copy number variation1nstd206human GRCh38 chr16: 30,556,439-30,561,776 , GRCh37.p13 chr16: 30,567,760-30,573,097 ZNF764
    nsv5187566mobile element insertion1nstd203human GRCh38 chr16: 30,552,396-30,552,407 , GRCh37.p13 chr16: 30,563,717-30,563,728 ZNF764
    nsv5186747mobile element insertion1nstd203human GRCh38 chr16: 30,552,392-30,552,407 , GRCh37.p13 chr16: 30,563,713-30,563,728 ZNF764
    nsv5183324mobile element insertion1nstd203human GRCh38 chr16: 30,552,391-30,552,407 , GRCh37.p13 chr16: 30,563,712-30,563,728 ZNF764
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4856813copy number variation1nstd200human GRCh37 chr16: 30,562,924-30,563,529 , GRCh38.p12 chr16: 30,551,603-30,552,208 ZNF764
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4554059insertion1nstd166human GRCh37.p13 chr16: 30,563,712-30,563,712 , GRCh38.p12 chr16: 30,552,391-30,552,391 ZNF764
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4244644copy number variation1nstd166human GRCh37.p13 chr16: 30,568,221-30,573,097 , GRCh38.p12 chr16: 30,556,900-30,561,776 ZNF764
    nsv4244120copy number variation1nstd166human GRCh37.p13 chr16: 30,568,210-30,576,358 , GRCh38.p12 chr16: 30,556,889-30,565,037 ZNF764
    nsv4237523copy number variation1nstd166human GRCh37.p13 chr16: 30,569,874-30,569,952 , GRCh38.p12 chr16: 30,558,553-30,558,631 ZNF764
    nsv3924250copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,828,435-31,357,519 , GRCh37 chr16: 29,920,934-31,450,018 , GRCh38 chr16: 29,909,613-31,438,697 MIR4518, ZNF747-DT, 95 more genes
    nsv3918040copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,370,550-30,581,820 , NCBI36 chr16: 30,278,051-30,489,321 , GRCh38 chr16: 30,359,229-30,570,499 RPL7L1P16, SEPHS2, 15 more genes
    nsv3916220copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,059,290-30,643,566 , NCBI36 chr16: 22,966,791-30,551,067 , GRCh38 chr16: 23,047,969-30,632,245 MIR548W, SLX1A-SULT1A3, 196 more genes
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