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Items: 1 to 20 of 54

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4455234copy number variation1nstd102humanPathogenic GRCh37 chr8: 48,730,498-48,829,786 , GRCh38.p12 chr8: 47,817,937-47,917,226 PRKDC
    nsv4683039copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,714-48,711,971 , GRCh38.p12 chr8: 47,774,153-47,799,410 PRKDC
    nsv7097664copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,761,695-48,766,795 , GRCh38.p12 chr8: 47,849,134-47,854,234 PRKDC
    nsv6312725copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,689,385-48,732,091 , GRCh38.p12 chr8: 47,776,824-47,819,530 PRKDC
    nsv5381478copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,714-48,713,567 , GRCh38.p12 chr8: 47,774,153-47,801,006 PRKDC
    nsv5564477copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,714-48,701,819 , GRCh38.p12 chr8: 47,774,153-47,789,258 PRKDC
    nsv6312829copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,734-48,691,674 , GRCh38.p12 chr8: 47,774,173-47,779,113 PRKDC
    nsv4682169copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,866,160-48,872,706 , GRCh38.p12 chr8: 47,953,600-47,960,146 PRKDC, MCM4
    nsv3896828copy number variation1nstd102humanBenign GRCh37 chr8: 48,684,355-48,890,009 , GRCh38.p12 chr8: 47,771,794-47,977,449 PRKDC, RNU6-519P, 2 more genes
    nsv3902481copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,587,984-48,780,185 , GRCh38.p12 chr8: 47,675,422-47,867,624 PRKDC, CEBPD, 1 more genes
    nsv7097663copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,734-48,872,686 , GRCh38.p12 chr8: 47,774,173-47,960,126 PRKDC, LOC105375818, 1 more genes
    nsv4456867copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,746,598-48,883,437 , GRCh38.p12 chr8: 47,834,037-47,970,877 PRKDC, LOC105375818, 1 more genes
    nsv4729461copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,671,451-48,889,259 , GRCh38.p12 chr8: 47,758,889-47,976,699 PRKDC, MCM4, 1 more genes
    nsv3913445copy number variation1nstd102humanUncertain significance GRCh38 chr8: 47,701,537-47,918,282 , GRCh37 chr8: 48,614,099-48,830,842 , NCBI36 chr8: 48,776,652-48,993,395 PRKDC, CEBPD, 1 more genes
    nsv4450030copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,714-48,872,706 , GRCh38.p12 chr8: 47,774,153-47,960,146 PRKDC, MCM4, 1 more genes
    nsv6312726copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,769,697-48,889,338 , GRCh38.p12 chr8: 47,857,136-47,976,778 PRKDC, LOC105375818, 1 more genes
    nsv6312830copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,845,560-48,889,338 , GRCh38.p12 chr8: 47,933,000-47,976,778 PRKDC, LOC105375818, 1 more genes
    nsv5381645copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,839,734-48,872,706 , GRCh38.p12 chr8: 47,927,174-47,960,146 PRKDC, LOC105375818, 1 more genes
    nsv4681312copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,845,560-48,872,706 , GRCh38.p12 chr8: 47,933,000-47,960,146 PRKDC, LOC105375818, 1 more genes
    nsv4452294copy number variation1nstd102humanPathogenic GRCh37 chr8: 48,270,390-49,987,806 , GRCh38.p12 chr8: 47,357,823-49,075,247 PRKDC, LOC100420532, 29 more genes
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