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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053923inversion1nstd229human GRCh38 chr4: 143,521,980-150,843,613 , GRCh37.p13 chr4: 144,443,133-151,764,765 AKIRIN2P1, PRMT9, 87 more genes
    nsv7050914inversion1nstd229human GRCh38 chr4: 143,519,295-150,840,265 , GRCh37.p13 chr4: 144,440,448-151,761,417 MIR548G, LOC100420464, 87 more genes
    nsv6757899copy number variation1nstd229human GRCh38 chr4: 145,634,532-145,638,587 , GRCh37.p13 chr4: 146,555,684-146,559,739 MMAA
    nsv6757414copy number variation1nstd229human GRCh38 chr4: 145,644,701-145,681,300 , GRCh37.p13 chr4: 146,565,853-146,602,452 C4orf51, MMAA
    nsv6755849copy number variation1nstd229human GRCh38 chr4: 145,605,358-145,625,737 , GRCh37.p13 chr4: 146,526,510-146,546,889 NCOA4P3, MMAA
    nsv6755106copy number variation1nstd229human GRCh38 chr4: 145,618,532-145,623,642 , GRCh37.p13 chr4: 146,539,684-146,544,794 NCOA4P3, MMAA
    nsv6752156copy number variation1nstd229human GRCh38 chr4: 145,624,034-145,629,068 , GRCh37.p13 chr4: 146,545,186-146,550,220 NCOA4P3, MMAA
    nsv6747291copy number variation1nstd229human GRCh38 chr4: 145,559,185-145,731,914 , GRCh37.p13 chr4: 146,480,337-146,653,066 SMAD1, LOC285422, 4 more genes
    nsv6746317copy number variation1nstd229human GRCh38 chr4: 145,568,501-145,635,200 , GRCh37.p13 chr4: 146,489,653-146,556,352 NCOA4P3, LOC285422, 2 more genes
    nsv6741306copy number variation1nstd229human GRCh38 chr4: 145,659,481-145,670,029 , GRCh37.p13 chr4: 146,580,633-146,591,181 MMAA
    nsv6565024inversion1nstd223human GRCh38 chr4: 145,648,436-145,648,938 , GRCh37.p13 chr4: 146,569,588-146,570,090 MMAA
    nsv6394533copy number variation1nstd223human GRCh38 chr4: 145,605,358-145,625,737 , GRCh37.p13 chr4: 146,526,510-146,546,889 NCOA4P3, MMAA
    nsv6390510copy number variation1nstd223human GRCh38 chr4: 145,614,201-145,622,900 , GRCh37.p13 chr4: 146,535,353-146,544,052 NCOA4P3, MMAA
    nsv6378471copy number variation1nstd223human GRCh38 chr4: 140,215,978-145,835,229 , GRCh37.p13 chr4: 141,137,132-146,756,381 OTUD4, GYPA, 62 more genes
    nsv6376034copy number variation1nstd223human GRCh38 chr4: 145,624,033-145,629,066 , GRCh37.p13 chr4: 146,545,185-146,550,218 NCOA4P3, MMAA
    nsv6312237copy number variation1nstd102humanPathogenic GRCh37 chr4: 146,575,136-146,576,596 , GRCh38.p12 chr4: 145,653,984-145,655,444 MMAA
    nsv6311715copy number variation1nstd102humanPathogenic GRCh37 chr4: 146,560,292-149,358,012 , GRCh38.p12 chr4: 145,639,140-148,436,860 PRMT5P1, LOC105377472, 32 more genes
    nsv6255466mobile element insertion1nstd215human GRCh38 chr4: 145,641,484-145,641,484 , GRCh37.p13 chr4: 146,562,636-146,562,636 MMAA
    nsv6255465mobile element insertion1nstd215human GRCh38 chr4: 145,627,272-145,627,272 , GRCh37.p13 chr4: 146,548,424-146,548,424 MMAA
    nsv6255464mobile element insertion1nstd215human GRCh38 chr4: 145,622,858-145,622,858 , GRCh37.p13 chr4: 146,544,010-146,544,010 NCOA4P3, MMAA
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