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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095158copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,061,310-41,061,445 , GRCh38.p12 chr17: 42,909,293-42,909,428 G6PC1
    nsv7095157copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,055,928-41,056,246 , GRCh38.p12 chr17: 42,903,911-42,904,229 G6PC1
    nsv7095156copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,894-41,063,443 , GRCh38.p12 chr17: 42,900,877-42,911,426 G6PC1
    nsv7095155copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,894-41,056,246 , GRCh38.p12 chr17: 42,900,877-42,904,229 G6PC1
    nsv7095154copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,052,894-41,053,143 , GRCh38.p12 chr17: 42,900,877-42,901,126 G6PC1
    nsv7094975copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,052,894-41,154,937 , GRCh38.p12 chr17: 42,900,877-43,002,920 RPL27, G6PC1, 5 more genes
    nsv7094974copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,894-41,059,665 , GRCh38.p12 chr17: 42,900,877-42,907,648 G6PC1
    nsv7094887copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,059,520-41,063,443 , GRCh38.p12 chr17: 42,907,503-42,911,426 G6PC1
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 more genes
    nsv6985364copy number variation1nstd229human GRCh38 chr17: 42,723,977-42,924,183 , GRCh37.p13 chr17: 40,875,995-41,076,200 AOC2, WNK4, 15 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6495725copy number variation1nstd223human GRCh38 chr17: 42,904,887-42,947,632 , GRCh37.p13 chr17: 41,056,904-41,099,649 RNY4P2, G6PC1
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 more genes
    nsv5938206copy number variation1nstd209human GRCh38 chr17: 42,904,920-42,905,352 , GRCh37.p13 chr17: 41,056,937-41,057,369 G6PC1
    nsv5673118copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,059,530-41,059,655 , GRCh38.p12 chr17: 42,907,513-42,907,638 G6PC1
    nsv5673099copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,053,048-41,053,049 , GRCh38 chr17: 42,901,031-42,901,032 G6PC1
    nsv5672880copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,055,938-41,063,453 , GRCh38.p12 chr17: 42,903,921-42,911,436 G6PC1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5526220copy number variation1nstd206human GRCh38 chr17: 42,904,922-42,905,353 , GRCh37.p13 chr17: 41,056,939-41,057,370 G6PC1
    nsv5203218mobile element deletion1nstd204human GRCh38.p13 chr17: 42,914,576-42,914,929 , GRCh37.p13 chr17: 41,066,593-41,066,946 G6PC1
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