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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094579copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,712,146-31,021,717 , GRCh38.p12 chr16: 30,700,825-31,010,396 FBXL19-AS1, BCL7C, 19 more genes
    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
    nsv6996095copy number variation1nstd229human GRCh38 chr16: 30,970,801-30,978,100 , GRCh37.p13 chr16: 30,982,122-30,989,421 SETD1A
    nsv6992975copy number variation1nstd229human GRCh38 chr16: 30,972,601-30,979,100 , GRCh37.p13 chr16: 30,983,922-30,990,421 SETD1A
    nsv6992677copy number variation1nstd229human GRCh38 chr16: 30,859,398-31,135,376 , GRCh37.p13 chr16: 30,870,719-31,146,697 SETD1A, HSD3B7, 19 more genes
    nsv6990871copy number variation1nstd229human GRCh38 chr16: 30,902,101-31,224,500 , GRCh37.p13 chr16: 30,913,422-31,235,821 CTF2P, VKORC1, 22 more genes
    nsv6988371copy number variation1nstd229human GRCh38 chr16: 30,972,001-30,978,100 , GRCh37.p13 chr16: 30,983,322-30,989,421 SETD1A
    nsv6986614copy number variation1nstd229human GRCh38 chr16: 30,971,401-30,977,900 , GRCh37.p13 chr16: 30,982,722-30,989,221 SETD1A
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6512823copy number variation1nstd223human GRCh38 chr16: 30,956,701-30,958,200 , GRCh37.p13 chr16: 30,968,022-30,969,521 SETD1A
    nsv6511551copy number variation1nstd223human GRCh38 chr16: 30,972,397-30,978,089 , GRCh37.p13 chr16: 30,983,718-30,989,410 SETD1A
    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
    nsv5934387copy number variation1nstd209human GRCh38 chr16: 30,972,397-30,978,088 , GRCh37.p13 chr16: 30,983,718-30,989,409 SETD1A
    nsv5881502copy number variation1nstd209human GRCh38 chr16: 30,972,351-30,978,044 , GRCh37.p13 chr16: 30,983,672-30,989,365 SETD1A
    nsv5531777copy number variation1nstd206human GRCh38 chr16: 30,972,397-30,978,089 , GRCh37.p13 chr16: 30,983,718-30,989,410 SETD1A
    nsv5520399copy number variation1nstd206human GRCh38 chr16: 30,955,365-30,955,485 , GRCh37.p13 chr16: 30,966,686-30,966,806 SETD1A, ORAI3
    nsv5331828translocation1nstd200human GRCh37 chr16: 30,989,410-30,989,410 , GRCh37 chr16: 30,983,718-30,983,718 , GRCh38.p12 chr16: 30,978,089-30,978,089 , GRCh38.p12 chr16: 30,972,397-30,972,397 SETD1A
    nsv5309308copy number variation1nstd204human GRCh38.p13 chr16: 30,972,369-30,978,115 , GRCh37.p13 chr16: 30,983,690-30,989,436 SETD1A
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