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Items: 1 to 20 of 265

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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
    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
    nsv6992575copy number variation1nstd229human GRCh38 chr16: 30,487,431-30,487,971 , GRCh37.p13 chr16: 30,498,752-30,499,292 ITGAL
    nsv6988807copy number variation1nstd229human GRCh38 chr16: 30,487,142-30,487,913 , GRCh37.p13 chr16: 30,498,463-30,499,234 ITGAL
    nsv6978803copy number variation1nstd229human GRCh38 chr16: 30,515,015-30,518,082 , GRCh37.p13 chr16: 30,526,336-30,529,403 ITGAL
    nsv6978096copy number variation1nstd229human GRCh38 chr16: 30,489,644-30,490,311 , GRCh37.p13 chr16: 30,500,965-30,501,632 ITGAL
    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
    nsv6623595copy number variation1nstd224human GRCh37 chr16: 30,510,489-30,521,792 , GRCh38.p12 chr16: 30,499,168-30,510,471 MIR4518, ITGAL
    nsv6595364inversion1nstd223human GRCh38 chr16: 30,512,297-30,513,007 , GRCh37.p13 chr16: 30,523,618-30,524,328 ITGAL
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6582466inversion1nstd223human GRCh38 chr16: 30,507,400-30,507,983 , GRCh37.p13 chr16: 30,518,721-30,519,304 ITGAL
    nsv6581468inversion1nstd223human GRCh38 chr16: 30,500,097-30,501,627 , GRCh37.p13 chr16: 30,511,418-30,512,948 ITGAL
    nsv6578680inversion1nstd223human GRCh38 chr16: 30,497,077-30,497,776 , GRCh37.p13 chr16: 30,508,398-30,509,097 ITGAL
    nsv6576072inversion1nstd223human GRCh38 chr16: 30,495,677-30,496,796 , GRCh37.p13 chr16: 30,506,998-30,508,117 ITGAL
    nsv6506640copy number variation1nstd223human GRCh38 chr16: 30,497,898-30,498,852 , GRCh37.p13 chr16: 30,509,219-30,510,173 ITGAL
    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
    nsv6288707insertion1nstd214human GRCh38 chr16: 30,499,715-30,499,715 , GRCh37.p13 chr16: 30,511,036-30,511,036 ITGAL
    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
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