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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113647copy number variation1nstd186human GRCh37 chr16: 14,781,857-14,855,857 , GRCh38.p12 chr16|NT_187607.1: 291,719-557,969 , GRCh38.p12 chr16: 14,688,000-14,762,000 , PKD1P6-NPIPP1, 14 more genes
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv6112799copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,089,795-2,185,919 , GRCh38.p12 chr16: 2,039,794-2,135,918 NTHL1, PKD1, 6 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv6112776copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,140,783-2,187,415 , GRCh38.p12 chr16: 2,090,782-2,137,414 PKD1, MIR1225, 4 more genes
    nsv5672839copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,103,323-2,185,710 , GRCh38.p12 chr16: 2,053,322-2,135,709 PKD1, TSC2, 5 more genes
    nsv5672753copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,182,491-2,188,216 , GRCh38 chr16: 2,132,490-2,138,215 PKD1, MIR3180-5, 1 more genes
    nsv5380995copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978 TEDC2, MIR3677HG, 33 more genes
    nsv5271137copy number variation1nstd204human GRCh38.p13 chr16: 1,615,401-2,135,300 , GRCh37.p13 chr16: 1,665,402-2,185,301 SNHG9, SNORA64, 40 more genes
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5266471copy number variation1nstd204human GRCh38.p13 chr16: 1,936,501-2,552,200 , GRCh37.p13 chr16: 1,986,502-2,602,201 AMDHD2, MIR3178, 56 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
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4716573copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,157,801-2,288,100 , GRCh38.p12 chr16: 2,107,800-2,238,099 MIR3180-5, BRICD5, 12 more genes
    nsv4685870copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,165,147-2,202,323 , GRCh38.p12 chr16: 2,115,146-2,152,322 PKD1, MIR3180-5, 2 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
    nsv4681114copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,098,597-2,185,710 , GRCh38.p12 chr16: 2,048,596-2,135,709 PKD1, TSC2, 5 more genes
    nsv4676093copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,893,566-16,330,627 , GRCh38.p12 chr16: 14,799,709-16,236,770 , GRCh38.p12 chr16|NT_187607.1: 333,436-1,894,768 MIR3180-4, ABCC1, 51 more genes
    nsv4675592copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,780,543-16,391,045 , GRCh38.p12 chr16: 14,686,686-16,297,188 , GRCh38.p12 chr16|NT_187607.1: 259,545-1,955,193 PLA2G10, MIR3180-4, 55 more genes
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