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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683474copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,740-2,729,727 , GRCh38.p12 chr9: 2,717,740-2,729,727 KCNV2
    nsv7097950copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,755-2,728,666 , GRCh38.p12 chr9: 2,717,755-2,728,666 KCNV2
    nsv7097951copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,758-2,728,666 , GRCh38.p12 chr9: 2,717,758-2,728,666 KCNV2
    nsv7098079copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,738-2,719,115 , GRCh38.p12 chr9: 2,717,738-2,719,115 KCNV2
    nsv5673821copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,729,426-2,729,727 , GRCh38.p12 chr9: 2,729,426-2,729,727 KCNV2
    nsv7093337copy number variation1nstd102humanPathogenic GRCh38 chr9: 2,718,842-2,718,929 , GRCh37 chr9: 2,718,842-2,718,929 KCNV2
    nsv6289895copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 2,716,981-2,787,016 , GRCh38.p12 chr9: 2,716,981-2,787,016 KCNV2
    nsv3905641copy number variation1nstd102humanLikely benign GRCh37 chr9: 2,689,263-2,787,884 , GRCh38.p12 chr9: 2,689,263-2,787,884 KCNV2
    nsv3913501copy number variation1nstd102humanUncertain significance NCBI36 chr9: 2,672,523-2,774,028 , GRCh37 chr9: 2,682,523-2,784,028 , GRCh38 chr9: 2,682,523-2,784,028 KCNV2
    nsv6637550copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,683,132-2,847,102 , GRCh38.p12 chr9: 2,683,132-2,847,102 KCNV2, PUM3
    nsv3890749copy number variation1nstd102humanLikely benign GRCh37 chr9: 2,689,263-3,073,977 , GRCh38.p12 chr9: 2,689,263-3,073,977 KCNV2, CARM1P1, 3 more genes
    nsv4675737copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,549,592-2,788,241 , GRCh38.p12 chr9: 2,549,592-2,788,241 KCNV2, VLDLR-AS1, 2 more genes
    nsv6313769copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,630,683-2,841,614 , GRCh38.p12 chr9: 2,630,683-2,841,614 KCNV2, VLDLR, 2 more genes
    nsv3896357copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,639,829-2,717,874 , GRCh38.p12 chr9: 2,639,829-2,717,874 KCNV2, VLDLR, 1 more genes
    nsv4675206copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,582,103-2,828,969 , GRCh38.p12 chr9: 2,582,103-2,828,969 KCNV2, VLDLR, 3 more genes
    nsv7097718copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,622,190-2,729,727 , GRCh38.p12 chr9: 2,622,190-2,729,727 KCNV2, VLDLR, 2 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 KCNV2, RPL4P5, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 KCNV2, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 KCNV2, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 KCNV2, DOCK8-AS1, 186 more genes
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