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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv6997912copy number variation1nstd229human GRCh38 chr16: 31,434,502-31,437,343 , GRCh37.p13 chr16: 31,445,823-31,448,664 ZNF843
    nsv6991338copy number variation1nstd229human GRCh38 chr16: 31,324,840-31,575,158 , GRCh37.p13 chr16: 31,336,161-31,586,479 YBX3P1, COX6A2, 14 more genes
    nsv6980127copy number variation1nstd229human GRCh38 chr16: 31,261,410-31,863,261 , GRCh37.p13 chr16: 31,272,731-31,874,582 ITGAM, FRG2KP, 24 more genes
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133022copy number variation1nstd213human GRCh37 chr16: 30,300,000-32,030,001 , GRCh38.p12 chr16: 30,288,679-32,018,680 COX6A2, CTF1, 91 more genes
    nsv6132985copy number variation1nstd213human GRCh37 chr16: 31,360,000-31,470,001 , GRCh38.p12 chr16: 31,348,679-31,458,680 COX6A2, ITGAD, 4 more genes
    nsv6132984copy number variation1nstd213human GRCh37 chr16: 31,340,000-32,080,001 , GRCh38.p12 chr16: 31,328,679-32,068,680 COX6A2, ITGAD, 31 more genes
    nsv5722275mobile element insertion1nstd211human GRCh38 chr16: 31,441,869-31,441,869 , GRCh37.p13 chr16: 31,453,190-31,453,190 ZNF843
    nsv5517923copy number variation1nstd206human GRCh38 chr16: 31,437,617-31,440,520 , GRCh37.p13 chr16: 31,448,938-31,451,841 ZNF843
    nsv5374704translocation1nstd200human GRCh38 chr16: 31,442,132-31,442,132 , GRCh38 chr19: 2,754,416-2,754,416 , GRCh37.p13 chr19: 2,754,414-2,754,414 , GRCh37.p13 chr16: 31,453,453-31,453,453 SGTA, ZNF843
    nsv5260631copy number variation1nstd204human GRCh38.p13 chr16: 31,437,626-31,440,399 , GRCh37.p13 chr16: 31,448,947-31,451,720 ZNF843
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv5003533copy number variation1nstd200human GRCh38 chr16: 31,434,546-31,437,343 , GRCh37.p13 chr16: 31,445,867-31,448,664 ZNF843
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4856847copy number variation1nstd200human GRCh37 chr16: 31,445,832-31,448,689 , GRCh38.p12 chr16: 31,434,511-31,437,368 ZNF843
    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
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