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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3874995copy number variation1nstd102humanBenign GRCh37 chr1: 180,739,039-180,755,321 , GRCh38.p12 chr1: 180,769,903-180,786,185 XPR1
    nsv3889758copy number variation1nstd102humanBenign GRCh37 chr1: 180,750,335-180,755,321 , GRCh38.p12 chr1: 180,781,199-180,786,185 XPR1
    nsv7095492copy number variation1nstd102humanUncertain significance GRCh37 chr1: 180,793,869-180,794,500 , GRCh38.p12 chr1: 180,824,733-180,825,364 XPR1
    nsv7095491copy number variation1nstd102humanUncertain significance GRCh37 chr1: 180,601,338-180,794,500 , GRCh38.p12 chr1: 180,632,202-180,825,364 XPR1
    nsv6310924copy number variation1nstd102humanUncertain significance GRCh37 chr1: 180,853,122-180,853,202 , GRCh38.p12 chr1: 180,883,986-180,884,066 XPR1
    nsv4453631copy number variation1nstd102humanUncertain significance GRCh37 chr1: 180,606,386-180,915,350 , GRCh38.p12 chr1: 180,637,250-180,946,214 XPR1, LOC107985231, 2 more genes
    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 XPR1, CRB1, 1608 more genes
    nsv3874431copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,990,029-195,086,758 , GRCh38.p12 chr1: 172,020,889-195,117,628 XPR1, PTGS2, 307 more genes
    nsv3873192copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589 XPR1, COLGALT2, 402 more genes
    nsv3888143copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609 XPR1, 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 XPR1, QSOX1, 263 more genes
    nsv3878624copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,073,386-200,192,265 , GRCh38.p12 chr1: 179,104,251-200,223,137 XPR1, LOC105371661, 249 more genes
    nsv3905741copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,002,040-199,694,025 , NCBI36 chr1: 177,268,663-197,960,648 , GRCh38 chr1: 179,032,905-199,724,897 XPR1, SLC4A1APP2, 240 more genes
    nsv3904393copy number variation1nstd102humanPathogenic GRCh37 chr1: 170,898,861-191,034,539 , GRCh38 chr1: 170,929,720-191,065,409 , NCBI36 chr1: 169,165,485-189,301,162 XPR1, RPL18P2, 302 more genes
    nsv3877653copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,011,314-199,022,759 , GRCh38.p12 chr1: 179,042,179-199,053,630 XPR1, LINC02818, 234 more genes
    nsv3896481copy number variation1nstd102humanPathogenic GRCh38 chr1: 176,595,962-196,301,688 , GRCh37 chr1: 176,565,098-196,270,818 , NCBI36 chr1: 174,831,721-194,537,441 XPR1, RN7SL230P, 231 more genes
    nsv3901149copy number variation1nstd102humanPathogenic NCBI36 chr1: 168,271,833-185,790,903 , GRCh37 chr1: 170,005,209-187,524,280 , GRCh38 chr1: 170,036,068-187,555,148 XPR1, RGSL1, 296 more genes
    nsv3886667copy number variation1nstd102humanPathogenic GRCh37 chr1: 173,131,908-187,406,532 , GRCh38.p12 chr1: 173,162,769-187,437,400 XPR1, CRYZL2P, 233 more genes
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 XPR1, LOC101928933, 148 more genes
    nsv3885424copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,873,155-181,823,980 , GRCh38.p12 chr1: 169,904,014-181,854,845 XPR1, TRUND-NNN7-1, 210 more genes
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