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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5941770copy number variation1nstd209human GRCh38 chr16: 14,964,786-15,043,270 , GRCh37.p13 chr16: 15,058,643-15,137,127 PDXDC1, NTAN1, 2 more genes
    nsv5939849copy number variation1nstd209human GRCh38 chr16: 15,049,744-15,050,023 , GRCh37.p13 chr16: 15,143,601-15,143,880 PDXDC1, NTAN1
    nsv5936572copy number variation1nstd209human GRCh38 chr16: 15,043,154-15,043,289 , GRCh37.p13 chr16: 15,137,011-15,137,146 PDXDC1, NTAN1
    nsv5879315copy number variation2nstd209human GRCh38 chr16: 15,030,379-15,038,512 , GRCh37.p13 chr16: 15,124,236-15,132,369 PDXDC1, NTAN1
    nsv5876139copy number variation2nstd209human GRCh38 chr16: 15,038,713-15,040,112 , GRCh37.p13 chr16: 15,132,570-15,133,969 NTAN1, PDXDC1
    nsv5873569copy number variation2nstd209human GRCh38 chr16: 15,047,064-15,082,042 , GRCh37.p13 chr16: 15,140,921-15,175,899 RRN3, PDXDC1, 1 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
    nsv5592627copy number variation1nstd207human GRCh38 chr16: 15,048,964-15,049,098 , GRCh37.p13 chr16: 15,142,821-15,142,955 NTAN1, PDXDC1
    nsv5529849copy number variation1nstd206human GRCh38 chr16: 15,049,745-15,050,024 , GRCh37.p13 chr16: 15,143,602-15,143,881 PDXDC1, NTAN1
    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
    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
    nsv5279197copy number variation1nstd204human GRCh38.p13 chr16: 15,042,613-15,043,863 , GRCh37.p13 chr16: 15,136,470-15,137,720 NTAN1, PDXDC1
    nsv5277614copy number variation1nstd204human GRCh38.p13 chr16: 15,029,999-15,054,810 , GRCh37.p13 chr16: 15,123,856-15,148,667 PDXDC1, NTAN1
    nsv5273127copy number variation1nstd204human GRCh38.p13 chr16: 15,044,464-15,045,563 , GRCh37.p13 chr16: 15,138,321-15,139,420 NTAN1, PDXDC1
    nsv5272946copy number variation1nstd204human GRCh38.p13 chr16: 15,030,546-15,038,112 , GRCh37.p13 chr16: 15,124,403-15,131,969 NTAN1, PDXDC1
    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
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