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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
    nsv6112786copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,124,782-16,291,779 , GRCh38.p12 chr16: 15,030,925-16,197,922 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,855,918 RNU6-213P, LOC105371102, 25 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5875686copy number variation1nstd209human GRCh38 chr16: 15,129,017-15,164,872 , GRCh37.p13 chr16: 15,222,874-15,258,729 PDXDC1, PKD1P6-NPIPP1, 3 more genes
    nsv5667163inversion1nstd207human GRCh38 chr16: 15,028,058-15,161,831 , GRCh37.p13 chr16: 15,121,915-15,255,688 PDXDC1, RRN3, 7 more genes
    nsv5602296copy number variation1nstd207human GRCh38 chr16: 15,154,971-15,155,977 , GRCh37.p13 chr16: 15,248,828-15,249,834 PKD1P6, MIR3180-4
    nsv5528797copy number variation1nstd206human GRCh38 chr16: 15,104,000-15,348,000 , GRCh37.p13 chr16: 15,197,857-15,441,857 , PDXDC1, 8 more genes
    nsv5528761copy number variation1nstd206human GRCh38 chr16: 15,030,500-15,224,000 , GRCh37.p13 chr16: 15,124,357-15,317,857 NTAN1, MIR3180-4, 8 more genes
    nsv5525731copy number variation1nstd206human GRCh38 chr16: 15,116,000-15,227,000 , GRCh37.p13 chr16: 15,209,857-15,320,857 PDXDC1, PKD1P6, 5 more genes
    nsv5381790copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,126,890-16,293,190 , GRCh38.p12 chr16: 15,033,033-16,199,333 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,857,331 RRN3, CEP20, 25 more genes
    nsv5380983copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,968,859-16,363,239 , GRCh38.p12 chr16: 14,875,002-16,269,382 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,927,385 LOC102724984, LOC728138, 50 more genes
    nsv5279999copy number variation1nstd204human GRCh38.p13 chr16: 15,154,742-15,156,538 , GRCh37.p13 chr16: 15,248,599-15,250,395 PKD1P6, MIR3180-4
    nsv5279310copy number variation1nstd204human GRCh38.p13 chr16: 15,139,301-15,211,900 , GRCh37.p13 chr16: 15,233,158-15,305,757 MIR3180-4, PKD1P6, 2 more genes
    nsv5277831copy number variation1nstd204human GRCh37.p13 chr16: 15,195,758-15,258,557 , GRCh38.p13 chr16: 15,101,901-15,164,700 PDXDC1, PKD1P6, 5 more genes
    nsv5270987copy number variation1nstd204human GRCh38.p13 chr16: 15,030,401-15,218,400 , GRCh37.p13 chr16: 15,124,258-15,312,257 LOC105371096, NPIPP1, 8 more genes
    nsv5264647copy number variation1nstd204human GRCh38.p13 chr16: 15,139,401-15,164,700 , GRCh37.p13 chr16: 15,233,258-15,258,557 PKD1P6, MIR3180-4, 1 more genes
    nsv5261879copy number variation1nstd204human GRCh37.p13 chr16: 15,208,293-15,258,729 , GRCh38.p13 chr16: 15,114,436-15,164,872 PDXDC1, PKD1P6, 4 more genes
    nsv5200385copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,048,751-16,292,235 , GRCh38.p12 chr16|NT_187607.1: 794,228-1,856,374 , GRCh38.p12 chr16: 14,954,894-16,198,378 MIR3179-1, RPL17P40, 33 more genes
    nsv5060037copy number variation1nstd102humanrisk factor GRCh37 chr16: 14,968,855-16,251,122 , GRCh38.p12 chr16: 14,874,998-16,157,265 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,815,194 NPIPA5, MIR1972-1, 48 more genes
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