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Items: 1 to 20 of 128

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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
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6990962copy number variation1nstd229human GRCh38 chr16: 30,414,791-30,414,847 , GRCh37.p13 chr16: 30,426,112-30,426,168 ZNF771
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 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
    nsv6506141copy number variation1nstd223human GRCh38 chr16: 30,417,201-30,418,300 , GRCh37.p13 chr16: 30,428,522-30,429,621 SNORA80C, ZNF771
    nsv6504300copy number variation1nstd223human GRCh38 chr16: 30,416,701-30,418,700 , GRCh37.p13 chr16: 30,428,022-30,430,021 ZNF771, SNORA80C
    nsv6290347copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,808,153-30,750,270 , GRCh38.p12 chr16: 29,796,832-30,738,949 SULT1A3, SEPHS2, 65 more genes
    nsv6290281copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 29,974,415-30,596,982 , GRCh38.p12 chr16: 29,963,094-30,585,661 ALDOA, SEPTIN1, 44 more genes
    nsv6199367copy number variation1nstd214human GRCh38 chr16: 30,410,843-30,410,898 , GRCh37.p13 chr16: 30,422,164-30,422,219 ZNF771
    nsv6196541copy number variation1nstd214human GRCh38 chr16: 30,414,791-30,414,846 , GRCh37.p13 chr16: 30,426,112-30,426,167 ZNF771
    nsv6145497copy number variation1nstd206human GRCh38 chr16: 30,390,486-30,406,486 , GRCh37.p13 chr16: 30,401,807-30,417,807 ZNF48, ZNF771
    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
    nsv5938613copy number variation1nstd209human GRCh38 chr16: 30,414,791-30,414,846 , GRCh37.p13 chr16: 30,426,112-30,426,167 ZNF771
    nsv5559509sequence alteration1nstd206human GRCh38 chr16: 30,417,625-30,419,422 , GRCh37.p13 chr16: 30,428,946-30,430,743 ZNF771, SNORA80C
    nsv5523799copy number variation1nstd206human GRCh38 chr16: 30,417,856-30,417,916 , GRCh37.p13 chr16: 30,429,177-30,429,237 SNORA80C, ZNF771
    nsv5521623copy number variation1nstd206human GRCh38 chr16: 30,417,633-30,419,072 , GRCh37.p13 chr16: 30,428,954-30,430,393 ZNF771, SNORA80C
    nsv5516640copy number variation1nstd206human GRCh38 chr16: 30,414,793-30,414,847 , GRCh37.p13 chr16: 30,426,114-30,426,168 ZNF771
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
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