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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5575899copy number variation1nstd207human GRCh38 chr8: 65,616,970-65,617,092 , GRCh37.p13 chr8: 66,529,205-66,529,327 ARMC1
    nsv5490854copy number variation1nstd206human GRCh38 chr8: 65,616,977-65,617,064 , GRCh37.p13 chr8: 66,529,212-66,529,299 ARMC1
    nsv5485566copy number variation1nstd206human GRCh38 chr8: 65,622,746-65,623,393 , GRCh37.p13 chr8: 66,534,981-66,535,628 ARMC1
    nsv5303383copy number variation1nstd204human GRCh38.p13 chr8: 65,629,025-65,629,636 , GRCh37.p13 chr8: 66,541,260-66,541,871 ARMC1
    nsv5180496mobile element insertion1nstd203human GRCh38 chr8: 65,627,706-65,627,723 , GRCh37.p13 chr8: 66,539,941-66,539,958 ARMC1
    nsv5116296mobile element insertion1nstd203human GRCh38 chr8: 65,623,262-65,623,307 , GRCh37.p13 chr8: 66,535,497-66,535,542 ARMC1
    nsv5111645mobile element insertion1nstd203human GRCh38 chr8: 65,623,260-65,623,307 , GRCh37.p13 chr8: 66,535,495-66,535,542 ARMC1
    nsv5100109mobile element insertion1nstd203human GRCh38 chr8: 65,629,154-65,629,170 , GRCh37.p13 chr8: 66,541,389-66,541,405 ARMC1
    nsv4960682copy number variation1nstd200human GRCh38 chr8: 65,628,374-65,631,323 , GRCh37.p13 chr8: 66,540,609-66,543,558 ARMC1
    nsv4821765copy number variation1nstd200human GRCh37 chr8: 66,541,263-66,541,860 , GRCh38.p12 chr8: 65,629,028-65,629,625 ARMC1
    nsv4715638copy number variation1nstd195human GRCh37 chr8: 66,536,382-66,536,383 , GRCh38.p12 chr8: 65,624,147-65,624,148 ARMC1
    nsv4710113copy number variation1nstd195human GRCh37 chr8: 66,536,386-66,536,387 , GRCh38.p12 chr8: 65,624,151-65,624,152 ARMC1
    nsv4709255copy number variation1nstd195human GRCh37 chr8: 66,533,043-66,533,044 , GRCh38.p12 chr8: 65,620,808-65,620,809 ARMC1
    nsv4571377mobile element insertion1nstd166human GRCh37.p13 chr8: 66,523,547-66,523,547 , GRCh38.p12 chr8: 65,611,312-65,611,312 ARMC1
    nsv4564408mobile element insertion1nstd166human GRCh37.p13 chr8: 66,526,398-66,526,398 , GRCh38.p12 chr8: 65,614,163-65,614,163 ARMC1
    nsv4527131copy number variation1nstd166human GRCh37.p13 chr8: 66,534,860-66,535,553 , GRCh38.p12 chr8: 65,622,625-65,623,318 ARMC1
    nsv4457166copy number variation1nstd102humanUncertain significance GRCh37 chr8: 66,320,808-66,641,126 , GRCh38.p12 chr8: 65,408,573-65,728,891 LINC01299, ARMC1, 2 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456190copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,280,508-67,782,846 , GRCh38.p12 chr8: 64,367,951-66,870,611 BHLHE22-AS1, VCPIP1, 41 more genes
    nsv4387546copy number variation1nstd173human GRCh37 chr8: 65,023,339-68,301,135 , GRCh38.p12 chr8: 64,110,782-67,388,900 , LOC105375885, 56 more genes
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