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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942846copy number variation1nstd209human GRCh38 chr16: 30,522,754-30,523,468 , GRCh37.p13 chr16: 30,534,075-30,534,789 ZNF768, ITGAL
    nsv5559120sequence alteration1nstd206human GRCh38 chr16: 30,532,793-30,533,068 , GRCh37.p13 chr16: 30,544,114-30,544,389 ZNF747, ZNF768
    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
    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
    nsv4623762copy number variation1nstd183human GRCh37 chr16: 30,492,708-30,533,449 , GRCh38.p12 chr16: 30,481,387-30,522,128 RNU7-61P, MIR4518, 2 more genes
    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
    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
    nsv3914248copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,763,368-31,955,076 , GRCh38 chr16: 23,752,047-31,943,755 , NCBI36 chr16: 23,670,869-31,862,577 ZG16, TPRKBP2, 250 more genes
    nsv3913895copy number variation1nstd102humanPathogenic NCBI36 chr16: 24,289,454-33,830,560 , GRCh37.p13 chr16: 24,381,953-33,923,059 , GRCh38.p12 chr16: 24,370,632-34,120,592 ITGAL, CORO1A, 310 more genes
    nsv3911651copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,500,284-30,610,734 , GRCh38 chr16: 29,581,462-30,691,912 , GRCh37 chr16: 29,592,783-30,703,233 PPP4C, MVP-DT, 71 more genes
    nsv3910351copy number variation1nstd102humanPathogenic GRCh38 chr16: 27,311,746-31,193,406 , NCBI36 chr16: 27,230,568-31,112,228 , GRCh37 chr16: 27,323,067-31,204,727 BCL7C, RNU6-1043P, 171 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS53, LINC02134, 1868 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CKLF, NPIPP1, 1882 more genes
    nsv3905126copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,826,162-34,375,007 , GRCh38.p12 chr16: 28,814,841-35,140,636 ALDOA, ATP2A1, 255 more genes
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