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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146042insertion1nstd232human GRCh37.p13 chr3: 25,668,356-25,668,356 , GRCh38.p12 chr3: 25,626,865-25,626,865 TOP2B
    nsv7145115copy number variation1nstd232human GRCh37.p13 chr3: 25,668,165-25,668,261 , GRCh38.p12 chr3: 25,626,674-25,626,770 TOP2B
    nsv7144240copy number variation1nstd232human GRCh37.p13 chr3: 25,670,442-25,670,523 , GRCh38.p12 chr3: 25,628,951-25,629,032 TOP2B
    nsv7141992insertion1nstd232human GRCh37.p13 chr3: 25,671,649-25,671,649 , GRCh38.p12 chr3: 25,630,158-25,630,158 TOP2B
    nsv7138123insertion1nstd232human GRCh37.p13 chr3: 25,668,789-25,668,789 , GRCh38.p12 chr3: 25,627,298-25,627,298 TOP2B
    nsv7137590insertion1nstd232human GRCh37.p13 chr3: 25,662,308-25,662,308 , GRCh38.p12 chr3: 25,620,817-25,620,817 TOP2B
    nsv7096563copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,611,229-25,662,327 , GRCh38.p12 chr3: 25,569,738-25,620,836 RARB, TOP2B
    nsv7096562copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 25,470,223-25,824,881 , GRCh38.p12 chr3: 25,428,732-25,783,390 RARB, TOP2B, 6 more genes
    nsv7096458copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,642,571-25,642,736 , GRCh38.p12 chr3: 25,601,080-25,601,245 TOP2B
    nsv7054168inversion1nstd229human GRCh38 chr3: 25,646,569-25,646,599 , GRCh37.p13 chr3: 25,688,060-25,688,090 TOP2B
    nsv7047194inversion1nstd229human GRCh38 chr3: 25,627,778-25,628,222 , GRCh37.p13 chr3: 25,669,269-25,669,713 TOP2B
    nsv7043476inversion1nstd229human GRCh38 chr3: 25,606,412-25,606,452 , GRCh37.p13 chr3: 25,647,903-25,647,943 TOP2B
    nsv6715501copy number variation1nstd229human GRCh38 chr3: 24,933,260-25,871,078 , GRCh37.p13 chr3: 24,974,751-25,912,569 CRIP1P2, MIR4442, 14 more genes
    nsv6709344copy number variation1nstd229human GRCh38 chr3: 25,599,540-25,599,959 , GRCh37.p13 chr3: 25,641,031-25,641,450 TOP2B
    nsv6708988copy number variation1nstd229human GRCh38 chr3: 25,638,328-25,638,353 , GRCh37.p13 chr3: 25,679,819-25,679,844 TOP2B
    nsv6701452copy number variation1nstd229human GRCh38 chr3: 25,618,606-25,623,735 , GRCh37.p13 chr3: 25,660,097-25,665,226 TOP2B
    nsv6549410inversion1nstd223human GRCh38 chr3: 25,644,476-25,644,858 , GRCh37.p13 chr3: 25,685,967-25,686,349 TOP2B
    nsv6539660inversion1nstd223human GRCh38 chr3: 25,621,391-25,621,975 , GRCh37.p13 chr3: 25,662,882-25,663,466 TOP2B
    nsv6366951copy number variation1nstd223human GRCh38 chr3: 25,630,901-25,632,600 , GRCh37.p13 chr3: 25,672,392-25,674,091 TOP2B
    nsv6366360copy number variation1nstd223human GRCh38 chr3: 25,604,701-25,606,300 , GRCh37.p13 chr3: 25,646,192-25,647,791 TOP2B
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