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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673959copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,582,748-137,677,904 , GRCh38.p12 chr9: 134,690,902-134,786,058 COL5A1
    nsv3873632copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,690,892-134,763,757 , GRCh37 chr9: 137,582,738-137,655,603 COL5A1
    nsv4450901copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,582,748-137,619,253 , GRCh38 chr9: 134,690,902-134,727,407 COL5A1
    nsv3882305copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,645,560-137,650,136 , GRCh38 chr9: 134,753,714-134,758,290 COL5A1
    nsv7097701copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,591,735-137,593,199 , GRCh38.p12 chr9: 134,699,889-134,701,353 COL5A1
    nsv3875902copy number variation2nstd102humanPathogenic GRCh38 chr9: 134,699,889-134,700,142 , GRCh37 chr9: 137,591,735-137,591,988 COL5A1
    nsv3884496copy number variation2nstd102humanPathogenic GRCh37 chr9: 137,644,415-137,644,511 , GRCh38 chr9: 134,752,569-134,752,665 COL5A1
    nsv5673885copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,619,102-137,698,152 , GRCh38.p12 chr9: 134,727,256-134,806,306 COL5A1
    nsv3880944copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 137,617,195-137,619,147 , GRCh38 chr9: 134,725,349-134,727,301 COL5A1
    nsv7098436copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 137,676,815-137,677,914 , GRCh38.p12 chr9: 134,784,969-134,786,068 COL5A1
    nsv3881133copy number variation2nstd102humanLikely pathogenic GRCh37 chr9: 137,582,738-137,593,199 , GRCh38 chr9: 134,690,892-134,701,353 COL5A1
    nsv3898856copy number variation1nstd102humanBenign GRCh37 chr9: 137,648,314-137,664,433 , GRCh38.p12 chr9: 134,756,468-134,772,587 COL5A1
    nsv6137795copy number variation1nstd102humanBenign GRCh37 chr9: 137,690,416-137,690,499 , GRCh38 chr9: 134,798,570-134,798,653 COL5A1
    nsv6137684copy number variation1nstd102humanLikely benign GRCh38 chr9: 134,752,314-134,752,315 , GRCh37 chr9: 137,644,160-137,644,161 COL5A1
    nsv3880211copy number variation2nstd102humanUncertain significance GRCh37 chr9: 137,619,092-137,620,673 , GRCh38 chr9: 134,727,246-134,728,827 COL5A1
    nsv7098434copy number variation1nstd102humanUncertain significance GRCh37 chr9: 137,623,322-137,623,993 , GRCh38.p12 chr9: 134,731,476-134,732,147 COL5A1
    nsv3873473copy number variation2nstd102humanUncertain significance GRCh38 chr9: 134,690,892-134,691,099 , GRCh37 chr9: 137,582,738-137,582,945 COL5A1
    nsv5564454copy number variation1nstd102humanUncertain significance GRCh37 chr9: 137,619,102-137,619,253 , GRCh38.p12 chr9: 134,727,256-134,727,407 COL5A1
    nsv3889949copy number variation1nstd102humanUncertain significance GRCh37 chr9: 137,533,651-137,534,142 , GRCh38 chr9: 134,641,805-134,642,296 COL5A1
    nsv5564501copy number variation1nstd102humanUncertain significance GRCh37 chr9: 137,534,028-137,534,148 , GRCh38.p12 chr9: 134,642,182-134,642,302 COL5A1
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