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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5674327insertion1nstd102humanPathogenic GRCh37 chr7: 150,644,727-150,644,727 , GRCh38 chr7: 150,947,639-150,947,639 KCNH2
    nsv5673926copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,649,598-150,649,650 , GRCh38 chr7: 150,952,510-150,952,562 KCNH2
    nsv5673790copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,654,369-150,656,834 , GRCh38.p12 chr7: 150,957,281-150,959,746 KCNH2
    nsv5673789copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,644,406-150,644,976 , GRCh38.p12 chr7: 150,947,318-150,947,888 KCNH2
    nsv5673788copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,642,447-150,656,830 , GRCh38.p12 chr7: 150,945,359-150,959,742 KCNH2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381637copy number variation1nstd102humanUncertain significance GRCh37 chr7: 150,642,453-152,373,165 , GRCh38.p12 chr7: 150,945,365-152,676,080 WDR86-AS1, XRCC2, 44 more genes
    nsv5309834copy number variation1nstd204human GRCh38.p13 chr7: 150,919,962-151,152,701 , GRCh37.p13 chr7: 150,617,050-150,849,788 , TMUB1, 10 more genes
    nsv5257485copy number variation1nstd204human GRCh38.p13 chr7: 150,919,780-150,988,905 , GRCh37.p13 chr7: 150,616,868-150,685,993 KCNH2
    nsv5059999copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 150,644,251-150,645,365 , GRCh38 chr7: 150,947,163-150,948,277 KCNH2
    nsv5059948copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 150,644,458-150,644,459 , GRCh38 chr7: 150,947,370-150,947,371 KCNH2
    nsv4954072copy number variation1nstd200human GRCh38 chr7: 150,920,190-151,152,443 , GRCh37.p13 chr7: 150,617,278-150,849,530 , TMUB1, 10 more genes
    nsv4951255copy number variation1nstd200human GRCh38 chr7: 150,973,441-150,974,912 , GRCh37.p13 chr7: 150,670,529-150,672,000 KCNH2
    nsv4825432copy number variation1nstd200human GRCh37 chr7: 150,617,278-150,849,530 , GRCh38.p12 chr7: 150,920,190-151,152,443 , FASTK, 10 more genes
    nsv4754093inversion1nstd199human GRCh37 chr7: 149,731,009-153,760,532 , GRCh38.p12 chr7: 150,033,920-154,063,447 , AOC1, 98 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4684225copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,644,479-150,644,753 , GRCh38 chr7: 150,947,389-150,947,390 KCNH2
    nsv4683838copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr7: 150,642,443-151,385,353 , GRCh38.p12 chr7: 150,945,355-151,688,267 CDK5, MIR3907, 26 more genes
    nsv4683306copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,654,369-150,675,011 , GRCh38.p12 chr7: 150,957,281-150,977,923 KCNH2
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