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Items: 1 to 20 of 47

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880472copy number variation1nstd102humanBenign GRCh37 chr1: 179,461,671-179,469,314 , GRCh38.p12 chr1: 179,492,536-179,500,179 AXDND1
    nsv3887253copy number variation1nstd102humanBenign GRCh37 chr1: 179,329,878-179,334,934 , GRCh38.p12 chr1: 179,360,743-179,365,799 AXDND1
    nsv3878047copy number variation1nstd102humanBenign GRCh37 chr1: 179,453,424-179,457,465 , GRCh38.p12 chr1: 179,484,289-179,488,330 AXDND1
    nsv3887680copy number variation1nstd102humanBenign GRCh37 chr1: 179,454,136-179,457,465 , GRCh38.p12 chr1: 179,485,001-179,488,330 AXDND1
    nsv3877638copy number variation1nstd102humanBenign GRCh37 chr1: 179,455,645-179,459,720 , GRCh38.p12 chr1: 179,486,510-179,490,585 AXDND1
    nsv3889903copy number variation1nstd102humanBenign GRCh37 chr1: 179,455,645-179,458,821 , GRCh38.p12 chr1: 179,486,510-179,489,686 AXDND1
    nsv3878527copy number variation1nstd102humanBenign GRCh37 chr1: 179,456,776-179,459,720 , GRCh38.p12 chr1: 179,487,641-179,490,585 AXDND1
    nsv3878283copy number variation1nstd102humanBenign GRCh37 chr1: 179,455,645-179,458,472 , GRCh38.p12 chr1: 179,486,510-179,489,337 AXDND1
    nsv3876160copy number variation1nstd102humanBenign GRCh37 chr1: 179,455,769-179,458,472 , GRCh38.p12 chr1: 179,486,634-179,489,337 AXDND1
    nsv3884459copy number variation1nstd102humanBenign GRCh37 chr1: 179,456,190-179,458,821 , GRCh38.p12 chr1: 179,487,055-179,489,686 AXDND1
    nsv3870993copy number variation1nstd102humanBenign GRCh37 chr1: 179,457,276-179,459,720 , GRCh38.p12 chr1: 179,488,141-179,490,585 AXDND1
    nsv3880750copy number variation1nstd102humanBenign GRCh37 chr1: 179,456,190-179,458,472 , GRCh38.p12 chr1: 179,487,055-179,489,337 AXDND1
    nsv3889201copy number variation1nstd102humanBenign GRCh37 chr1: 179,456,359-179,458,472 , GRCh38.p12 chr1: 179,487,224-179,489,337 AXDND1
    nsv3886321copy number variation1nstd102humanBenign GRCh37 chr1: 179,457,276-179,458,821 , GRCh38.p12 chr1: 179,488,141-179,489,686 AXDND1
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 AXDND1, CRB1, 1608 more genes
    nsv3874431copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,990,029-195,086,758 , GRCh38.p12 chr1: 172,020,889-195,117,628 AXDND1, PTGS2, 307 more genes
    nsv3873192copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589 AXDND1, COLGALT2, 402 more genes
    nsv3888143copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609 AXDND1, CSRP1-AS1, 273 more genes
    nsv4673925copy number variation1nstd102humanPathogenic GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928 AXDND1, QSOX1, 263 more genes
    nsv3878624copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,073,386-200,192,265 , GRCh38.p12 chr1: 179,104,251-200,223,137 AXDND1, LOC105371661, 249 more genes
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