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Items: 1 to 20 of 94

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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
    nsv6995457copy number variation1nstd229human GRCh38 chr16: 30,562,041-30,598,716 , GRCh37.p13 chr16: 30,573,362-30,610,037 ZNF785, ZNF688
    nsv6992667copy number variation1nstd229human GRCh38 chr16: 30,517,701-30,585,900 , GRCh37.p13 chr16: 30,529,022-30,597,221 ZNF764, ZNF747-DT, 6 more genes
    nsv6637207copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,460,206-30,906,733 , GRCh38.p12 chr16: 30,448,885-30,895,412 ZNF629, ZNF689, 27 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
    nsv6508122copy number variation1nstd223human GRCh38 chr16: 30,565,008-30,578,175 , GRCh37.p13 chr16: 30,576,329-30,589,496 ZNF785, ZNF688
    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
    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
    nsv5518074copy number variation1nstd206human GRCh38 chr16: 30,571,449-30,577,660 , GRCh37.p13 chr16: 30,582,770-30,588,981 ZNF785, ZNF688
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv5003487copy number variation1nstd200human GRCh38 chr16: 30,566,795-30,568,313 , GRCh37.p13 chr16: 30,578,116-30,579,634 ZNF688
    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
    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
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