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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098845copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 28,649,089-28,649,191 , GRCh38 chr18: 31,069,123-31,069,225 DSC2
    nsv7095440copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,981-29,648,347 , GRCh38.p12 chr18: 31,068,015-32,068,384 RNU6-167P, LOC390846, 22 more genes
    nsv7095439copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,981-28,681,934 , GRCh38.p12 chr18: 31,068,015-31,101,971 DSCAS, DSC2
    nsv7095378copy number variation1nstd102humanPathogenic GRCh37 chr18: 28,681,846-28,681,934 , GRCh38.p12 chr18: 31,101,883-31,101,971 DSCAS, DSC2
    nsv7095377copy number variation1nstd102humanPathogenic GRCh37 chr18: 28,673,522-28,673,606 , GRCh38.p12 chr18: 31,093,559-31,093,643 DSC2
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7015674copy number variation1nstd229human GRCh38 chr18: 31,101,595-31,106,309 , GRCh37.p13 chr18: 28,681,558-28,686,272 DSC2, DSCAS
    nsv7011839copy number variation1nstd229human GRCh38 chr18: 29,648,720-31,204,673 , GRCh37.p13 chr18: 27,228,685-28,784,636 LOC105372045, DSC2, 7 more genes
    nsv7010972copy number variation1nstd229human GRCh38 chr18: 31,055,283-31,057,103 , GRCh37.p13 chr18: 28,635,249-28,637,069 DSC2
    nsv7008986copy number variation1nstd229human GRCh38 chr18: 31,101,515-31,101,579 , GRCh37.p13 chr18: 28,681,478-28,681,542 DSCAS, DSC2
    nsv7008075copy number variation1nstd229human GRCh38 chr18: 31,097,305-31,097,945 , GRCh37.p13 chr18: 28,677,268-28,677,908 DSC2
    nsv7007924copy number variation1nstd229human GRCh38 chr18: 31,049,301-31,060,600 , GRCh37.p13 chr18: 28,629,267-28,640,566 DSC2
    nsv7005856copy number variation1nstd229human GRCh38 chr18: 31,076,675-31,080,892 , GRCh37.p13 chr18: 28,656,641-28,660,858 DSC2
    nsv6637278copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,628,215-28,683,174 , GRCh38.p12 chr18: 31,048,249-31,103,211 DSCAS, DSC2
    nsv6624582copy number variation1nstd224human GRCh37 chr18: 28,597,270-29,027,889 , GRCh38.p12 chr18: 31,017,304-31,447,926 DSC1, DSG4, 8 more genes
    nsv6534715copy number variation1nstd223human GRCh38 chr18: 31,097,858-31,098,880 , GRCh37.p13 chr18: 28,677,821-28,678,843 DSC2
    nsv6534270copy number variation1nstd223human GRCh38 chr18: 29,648,720-31,204,673 , GRCh37.p13 chr18: 27,228,685-28,784,636 DSC2, DSCAS, 7 more genes
    nsv6531628copy number variation1nstd223human GRCh38 chr18: 31,055,557-31,060,432 , GRCh37.p13 chr18: 28,635,523-28,640,398 DSC2
    nsv6524546copy number variation1nstd223human GRCh38 chr18: 31,049,303-31,060,634 , GRCh37.p13 chr18: 28,629,269-28,640,600 DSC2
    nsv6523675copy number variation1nstd223human GRCh38 chr18: 31,097,147-31,097,940 , GRCh37.p13 chr18: 28,677,110-28,677,903 DSC2
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