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Items: 1 to 20 of 382

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137783copy number variation1nstd102humanBenign GRCh38 chr17: 80,090,387-80,090,449 , GRCh37 chr17: 78,064,186-78,064,248 CCDC40
    nsv6137748copy number variation1nstd102humanLikely benign GRCh38 chr17: 80,090,254-80,090,346 , GRCh37 chr17: 78,064,053-78,064,145 CCDC40
    nsv6137695copy number variation1nstd102humanLikely benign GRCh37 chr17: 78,063,952-78,064,015 , GRCh38 chr17: 80,090,153-80,090,216 CCDC40
    nsv5977934insertion1nstd209human GRCh38 chr17: 80,082,245-80,082,245 , GRCh37.p13 chr17: 78,056,044-78,056,044 CCDC40
    nsv5975455insertion1nstd209human GRCh38 chr17: 80,044,701-80,044,701 , GRCh37.p13 chr17: 78,018,500-78,018,500 CCDC40
    nsv5719514mobile element insertion2nstd211human GRCh38 chr17: 80,052,975-80,052,975 , GRCh37.p13 chr17: 78,026,774-78,026,774 CCDC40
    nsv5700281mobile element insertion1nstd211human GRCh38 chr17: 80,078,542-80,078,542 , GRCh37.p13 chr17: 78,052,341-78,052,341 CCDC40
    nsv5700154mobile element insertion2nstd211human GRCh38 chr17: 80,082,253-80,082,253 , GRCh37.p13 chr17: 78,056,052-78,056,052 CCDC40
    nsv5662161insertion1nstd207human GRCh38 chr17: 80,082,245-80,082,245 , GRCh37.p13 chr17: 78,056,044-78,056,044 CCDC40
    nsv5651842insertion1nstd207human GRCh38 chr17: 80,090,401-80,090,401 , GRCh37.p13 chr17: 78,064,200-78,064,200 CCDC40
    nsv5585986copy number variation1nstd207human GRCh38 chr17: 80,090,386-80,090,448 , GRCh37.p13 chr17: 78,064,185-78,064,247 CCDC40
    nsv5564160copy number variation1nstd102humanUncertain significance GRCh38 chr17: 80,090,269-80,090,354 , GRCh37 chr17: 78,064,068-78,064,153 CCDC40
    nsv5523733copy number variation1nstd206human GRCh38 chr17: 80,096,142-80,101,295 , GRCh37.p13 chr17: 78,069,941-78,075,094 CCDC40, MIR1268B, 1 more genes
    nsv5514971copy number variation1nstd206human GRCh38 chr17: 80,051,525-80,054,851 , GRCh37.p13 chr17: 78,025,324-78,028,650 CCDC40
    nsv5513945copy number variation1nstd206human GRCh38 chr17: 80,051,725-80,053,372 , GRCh37.p13 chr17: 78,025,524-78,027,171 CCDC40
    nsv5426955mobile element insertion1nstd206human GRCh38 chr17: 80,078,542-80,078,593 , GRCh37.p13 chr17: 78,052,341-78,052,392 CCDC40
    nsv5381256copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,071,024-78,073,594 , GRCh38.p12 chr17: 80,097,225-80,099,795 MIR1268B, CCDC40, 1 more genes
    nsv5328105copy number variation1nstd204human GRCh38.p13 chr17: 80,075,597-80,076,037 , GRCh37.p13 chr17: 78,049,396-78,049,836 CCDC40
    nsv5159552mobile element insertion1nstd203human GRCh38 chr17: 80,056,003-80,056,016 , GRCh37.p13 chr17: 78,029,802-78,029,815 CCDC40
    nsv5156910mobile element insertion1nstd203human GRCh38 chr17: 80,082,244-80,082,249 , GRCh37.p13 chr17: 78,056,043-78,056,048 CCDC40
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