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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3886489copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,642,044-150,675,402 , GRCh38 chr7: 150,944,956-150,978,314 KCNH2
    nsv4683306copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,654,369-150,675,011 , GRCh38.p12 chr7: 150,957,281-150,977,923 KCNH2
    nsv3872923copy number variation1nstd102humanPathogenic GRCh38 chr7: 150,944,956-150,959,736 , GRCh37 chr7: 150,642,044-150,656,824 KCNH2
    nsv5673788copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,642,447-150,656,830 , GRCh38.p12 chr7: 150,945,359-150,959,742 KCNH2
    nsv6312329copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,642,453-150,649,961 , GRCh38.p12 chr7: 150,945,365-150,952,873 KCNH2
    nsv3888682copy number variation1nstd102humanPathogenic GRCh38 chr7: 150,974,691-150,977,933 , GRCh37 chr7: 150,671,779-150,675,021 KCNH2
    nsv6312620copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,642,443-150,645,641 , GRCh38.p12 chr7: 150,945,355-150,948,553 KCNH2
    nsv7097873copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,654,359-150,657,201 , GRCh38.p12 chr7: 150,957,271-150,960,113 KCNH2
    nsv3874435copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,653,076-150,655,552 , GRCh38 chr7: 150,955,988-150,958,464 KCNH2
    nsv5673790copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,654,369-150,656,834 , GRCh38.p12 chr7: 150,957,281-150,959,746 KCNH2
    nsv6312330copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,653,066-150,655,041 , GRCh38.p12 chr7: 150,955,978-150,957,953 KCNH2
    nsv5673789copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,644,406-150,644,976 , GRCh38.p12 chr7: 150,947,318-150,947,888 KCNH2
    nsv7093283copy number variation1nstd102humanPathogenic GRCh38 chr7: 150,951,346-150,951,673 , GRCh37 chr7: 150,648,434-150,648,761 KCNH2
    nsv3874288copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,656,640-150,656,844 , GRCh38 chr7: 150,959,552-150,959,756 KCNH2
    nsv4450074copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,656,650-150,656,834 , GRCh38 chr7: 150,959,562-150,959,746 KCNH2
    nsv6634480copy number variation1nstd102humanPathogenic GRCh38 chr7: 150,974,747-150,974,813 , GRCh37 chr7: 150,671,835-150,671,901 KCNH2
    nsv5673926copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,649,598-150,649,650 , GRCh38 chr7: 150,952,510-150,952,562 KCNH2
    nsv2779217copy number variation1nstd45humanPathogenic GRCh37 chr7: 150,642,044-150,675,402 , GRCh38.p12 chr7: 150,944,956-150,978,314 KCNH2
    nsv7097352copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 150,642,453-150,675,001 , GRCh38.p12 chr7: 150,945,365-150,977,913 KCNH2
    nsv4684225copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,644,479-150,644,753 , GRCh38 chr7: 150,947,389-150,947,390 KCNH2
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