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Items: 1 to 20 of 1655

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1154323copy number variation1nstd45humanPathogenic GRCh38.p12 chr10: 78,033,760-78,056,813 , GRCh37 chr10: 79,793,518-79,816,571 RPS24
    nsv4685969copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 154,142,454-154,147,728 , GRCh38 chr1: 154,169,978-154,175,252 TPM3
    nsv6878756copy number variation1nstd229human GRCh38 chr10: 43,387,937-43,396,454 , GRCh37.p13 chr10: 43,883,385-43,891,902 HNRNPF
    nsv6896992copy number variation1nstd229human GRCh38 chr10: 43,387,938-43,394,629 , GRCh37.p13 chr10: 43,883,386-43,890,077 HNRNPF
    nsv6642472copy number variation1nstd229human GRCh38 chr1: 154,185,201-154,190,200 , GRCh37.p13 chr1: 154,157,677-154,162,676 TPM3
    nsv6642013copy number variation1nstd229human GRCh38 chr1: 154,184,901-154,189,000 , GRCh37.p13 chr1: 154,157,377-154,161,476 TPM3
    nsv6642471copy number variation1nstd229human GRCh38 chr1: 154,185,192-154,188,871 , GRCh37.p13 chr1: 154,157,668-154,161,347 TPM3
    nsv6642689copy number variation1nstd229human GRCh38 chr1: 154,185,216-154,188,873 , GRCh37.p13 chr1: 154,157,692-154,161,349 TPM3
    nsv6986920copy number variation1nstd229human GRCh38 chr17: 47,965,826-47,969,276 , GRCh37.p13 chr17: 46,043,192-46,046,642 CDK5RAP3
    nsv7014036copy number variation1nstd229human GRCh38 chr19: 583,452-586,840 , GRCh37.p13 chr19: 583,452-586,840 BSG
    nsv7000420copy number variation1nstd229human GRCh38 chr19: 582,175-585,240 , GRCh37.p13 chr19: 582,175-585,240 BSG
    nsv6982466copy number variation1nstd229human GRCh38 chr17: 47,976,961-47,979,069 , GRCh37.p13 chr17: 46,054,327-46,056,435 CDK5RAP3
    nsv7014882copy number variation1nstd229human GRCh38 chr19: 579,731-580,427 , GRCh37.p13 chr19: 579,731-580,427 BSG
    nsv6795605copy number variation1nstd229human GRCh38 chr6: 30,725,118-30,725,638 , GRCh37.p13 chr6: 30,692,895-30,693,415 TUBB
    nsv7003882copy number variation1nstd229human GRCh38 chr19: 577,924-578,030 , GRCh37.p13 chr19: 577,924-578,030 BSG
    nsv6624099copy number variation1nstd224human GRCh37 chr17: 46,042,327-46,052,901 , GRCh38.p12 chr17: 47,964,961-47,975,535 CDK5RAP3
    nsv7142317copy number variation1nstd232human GRCh37.p13 chr12: 98,995,057-98,995,142 , GRCh38.p12 chr12: 98,601,279-98,601,364 SLC25A3
    nsv6528343copy number variation1nstd223human GRCh38 chr19: 1,543,624-1,553,030 , GRCh37.p13 chr19: 1,543,623-1,553,029 MEX3D
    nsv6322164copy number variation1nstd223human GRCh38 chr1: 154,185,154-154,188,913 , GRCh37.p13 chr1: 154,157,630-154,161,389 TPM3
    nsv6528162copy number variation1nstd223human GRCh38 chr19: 583,452-586,840 , GRCh37.p13 chr19: 583,452-586,840 BSG
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