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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3879983copy number variation1nstd102humanBenign GRCh37 chr1: 98,155,074-98,170,206 , GRCh38.p12 chr1: 97,689,518-97,704,650 DPYD
    nsv3874174copy number variation1nstd102humanBenign GRCh37 chr1: 98,059,803-98,079,674 , GRCh38.p12 chr1: 97,594,247-97,614,118 DPYD
    nsv4451700copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,905,533-97,985,890 , GRCh38.p12 chr1: 97,439,977-97,520,334 DPYD
    nsv4454432copy number variation1nstd102humanPathogenic GRCh37 chr1: 97,757,431-97,798,061 , GRCh38.p12 chr1: 97,291,875-97,332,505 DPYD, DPYD-AS1
    nsv7137019copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 97,658,805-97,770,814 , GRCh38.p12 chr1: 97,193,249-97,305,258 DPYD, DPYD-AS1
    nsv3888465copy number variation1nstd102humanBenign GRCh37 chr1: 98,251,973-98,316,285 , GRCh38.p12 chr1: 97,786,417-97,850,729 DPYD, DPYD-AS2
    nsv3879835copy number variation1nstd102humanBenign GRCh37 chr1: 97,457,893-97,721,488 , GRCh38.p12 chr1: 96,992,337-97,255,932 DPYD, DPYD-AS1
    nsv3886593copy number variation1nstd102humanUncertain significance GRCh37 chr1: 98,031,183-98,144,976 , GRCh38.p12 chr1: 97,565,627-97,679,420 DPYD, RPL26P9
    nsv7098997copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,548,027-97,658,624 , GRCh38.p12 chr1: 97,082,471-97,193,068 DPYD, DPYD-AS1
    nsv3872965copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,545,589-97,594,994 , GRCh38.p12 chr1: 97,080,033-97,129,438 DPYD, DPYD-AS1
    nsv4728272copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,638,240-97,660,637 , GRCh38.p12 chr1: 97,172,684-97,195,081 DPYD, DPYD-AS1
    nsv4454927copy number variation1nstd102humanUncertain significance GRCh37 chr1: 98,036,616-98,250,754 , GRCh38.p12 chr1: 97,571,060-97,785,198 DPYD, RPL26P9
    nsv4578544copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 97,658,804-98,058,774 , GRCh38.p12 chr1: 97,193,248-97,593,218 DPYD, RPL26P9, 3 more genes
    nsv3878362copy number variation1nstd102humanBenign GRCh37 chr1: 98,191,375-98,327,831 , GRCh38.p12 chr1: 97,725,819-97,862,275 DPYD, LOC100419654, 1 more genes
    nsv4453094copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,646,028-98,052,358 , GRCh38.p12 chr1: 97,180,472-97,586,802 DPYD, LOC105378867, 3 more genes
    nsv3879253copy number variation1nstd102humanUncertain significance GRCh37 chr1: 98,103,843-98,351,211 , GRCh38.p12 chr1: 97,638,287-97,885,655 DPYD, DPYD-AS2, 1 more genes
    nsv3876283copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,876,522-98,103,813 , GRCh38.p12 chr1: 97,410,966-97,638,257 DPYD, SEC63P1, 1 more genes
    nsv4450591copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,874,956-98,098,498 , GRCh38.p12 chr1: 97,409,400-97,632,942 DPYD, RPL26P9, 1 more genes
    nsv3878877copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,744,762-97,952,905 , GRCh38.p12 chr1: 97,279,206-97,487,349 DPYD, LOC105378867, 1 more genes
    nsv3905587copy number variation1nstd102humanUncertain significance GRCh37 chr1: 97,883,261-98,384,614 , GRCh38 chr1: 97,417,705-97,919,058 , NCBI36 chr1: 97,655,849-98,157,202 DPYD, DPYD-AS2, 3 more genes
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