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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970939insertion1nstd209human GRCh38 chr17: 39,724,272-39,724,272 , GRCh37.p13 chr17: 37,880,525-37,880,525 ERBB2
    nsv5649311insertion1nstd207human GRCh38 chr17: 39,694,258-39,694,258 , GRCh37.p13 chr17: 37,850,511-37,850,511 ERBB2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5381009copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,856,492-37,884,297 , GRCh38.p12 chr17: 39,700,239-39,728,044 MIEN1, ERBB2, 1 more genes
    nsv5156864mobile element insertion1nstd203human GRCh38 chr17: 39,724,272-39,724,288 , GRCh37.p13 chr17: 37,880,525-37,880,541 ERBB2
    nsv5153215mobile element insertion1nstd203human GRCh38 chr17: 39,690,417-39,690,426 , GRCh37.p13 chr17: 37,846,670-37,846,679 ERBB2
    nsv5016300copy number variation1nstd200human GRCh38 chr17: 39,722,075-39,722,596 , GRCh37.p13 chr17: 37,878,328-37,878,849 ERBB2
    nsv5016299copy number variation1nstd200human GRCh38 chr17: 39,695,470-39,697,815 , GRCh37.p13 chr17: 37,851,723-37,854,068 ERBB2
    nsv5013682copy number variation1nstd200human GRCh38 chr17: 39,723,981-39,724,702 , GRCh37.p13 chr17: 37,880,234-37,880,955 MIR4728, ERBB2
    nsv4858774copy number variation1nstd200human GRCh37 chr17: 37,878,328-37,878,849 , GRCh38.p12 chr17: 39,722,075-39,722,596 ERBB2
    nsv4765858insertion1nstd199human GRCh37 chr17: 37,850,490-37,850,490 , GRCh38.p12 chr17: 39,694,237-39,694,237 ERBB2
    nsv4625569copy number variation1nstd183human GRCh37 chr17: 37,736,785-37,904,211 , GRCh38.p12 chr17: 39,580,532-39,747,958 ERBB2, PGAP3, 9 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4457589copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,190,609-37,868,002 , GRCh38.p12 chr17: 39,034,356-39,711,749 ERBB2, PGAP3, 23 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4262542copy number variation1nstd166human GRCh37.p13 chr17: 37,880,425-37,880,533 , GRCh38.p12 chr17: 39,724,172-39,724,280 ERBB2
    nsv4262475copy number variation1nstd166human GRCh37.p13 chr17: 37,850,471-37,850,577 , GRCh38.p12 chr17: 39,694,218-39,694,324 ERBB2
    nsv4259385copy number variation1nstd166human GRCh37.p13 chr17: 37,878,328-37,878,849 , GRCh38.p12 chr17: 39,722,075-39,722,596 ERBB2
    nsv3940888insertion1nstd167human GRCh37 chr17: 37,847,809-37,847,809 , GRCh38.p12 chr17: 39,691,556-39,691,556 ERBB2
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
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