U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 98

    loading data ...

    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
    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
    nsv6306269copy number variation1nstd186human GRCh37 chr16: 30,541,807-30,547,807 , GRCh38.p12 chr16: 30,530,486-30,536,486 ZNF747, ZNF768, 2 more genes
    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
    nsv6144604copy number variation1nstd206human GRCh38 chr16: 30,530,486-30,536,486 , GRCh37.p13 chr16: 30,541,807-30,547,807 ZNF768, ZNF747, 2 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
    nsv6036700copy number variation1nstd212human GRCh38 chr16: 30,527,448-30,529,670 , GRCh37.p13 chr16: 30,538,769-30,540,991 ZNF768, ZNF747
    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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center