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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5946927copy number variation1nstd209human GRCh38 chr16: 1,498,940-1,498,989 , GRCh37.p13 chr16: 1,548,941-1,548,990 TELO2
    nsv5593786copy number variation1nstd207human GRCh38 chr16: 1,507,811-1,507,872 , GRCh37.p13 chr16: 1,557,812-1,557,873 TELO2
    nsv5526133copy number variation1nstd206human GRCh38 chr16: 1,503,656-1,504,073 , GRCh37.p13 chr16: 1,553,657-1,554,074 TELO2
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5278705copy number variation1nstd204human GRCh38.p13 chr16: 1,376,101-1,511,800 , GRCh37.p13 chr16: 1,426,102-1,561,801 UNKL, IFT140, 9 more genes
    nsv5278593copy number variation1nstd204human GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501 , MIR662, 73 more genes
    nsv5278406copy number variation1nstd204human GRCh38.p13 chr16: 1,493,421-1,549,952 , GRCh37.p13 chr16: 1,543,422-1,599,953 IFT140, TMEM204, 1 more genes
    nsv5268810copy number variation1nstd204human GRCh38.p13 chr16: 1,493,901-1,584,100 , GRCh37.p13 chr16: 1,543,902-1,634,101 IFT140, TMEM204, 2 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5158526mobile element insertion1nstd203human GRCh38 chr16: 1,499,836-1,499,851 , GRCh37.p13 chr16: 1,549,837-1,549,852 TELO2
    nsv4748435copy number variation1nstd199human GRCh37 chr16: 1,554,600-1,554,697 , GRCh38.p12 chr16: 1,504,599-1,504,696 TELO2
    nsv4738401copy number variation1nstd199human GRCh37 chr16: 1,557,749-1,557,801 , GRCh38.p12 chr16: 1,507,748-1,507,800 TELO2
    nsv4729490copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,505,184-1,818,754 , GRCh38.p12 chr16: 1,455,183-1,768,753 MAPK8IP3, MAPK8IP3-AS1, 11 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4683390copy number variation1nstd102humanPathogenic GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004 MRPS34, HAGHL, 102 more genes
    nsv4683209copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709 TMEM204, UQCC4, 67 more genes
    nsv4682518copy number variation1nstd102humanUncertain significance GRCh37 chr16: 624,055-2,550,979 , GRCh38.p12 chr16: 574,055-2,500,978 C1QTNF8, NHERF2, 133 more genes
    nsv4681361copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,535,940-1,561,151 , GRCh38.p12 chr16: 1,485,939-1,511,150 IFT140, TELO2, 1 more genes
    nsv4631180copy number variation1nstd183human GRCh37 chr16: 1,550,153-1,550,464 , GRCh38.p12 chr16: 1,500,152-1,500,463 TELO2
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