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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3888692copy number variation1nstd102humanLikely pathogenic GRCh38 chr2: 177,895,779-177,946,731 , GRCh37.p13 chr2: 178,760,506-178,811,458 PDE11A
    nsv3879741copy number variation1nstd102humanBenign GRCh37 chr2: 178,717,517-178,741,538 , GRCh38.p12 chr2: 177,852,790-177,876,811 PDE11A
    nsv3875701copy number variation1nstd102humanBenign GRCh37 chr2: 178,838,521-178,857,155 , GRCh38.p12 chr2: 177,973,794-177,992,428 PDE11A
    nsv3875700copy number variation1nstd102humanBenign GRCh37 chr2: 178,838,191-178,849,529 , GRCh38.p12 chr2: 177,973,464-177,984,802 PDE11A
    nsv3876204copy number variation1nstd102humanBenign GRCh37 chr2: 178,837,796-178,848,700 , GRCh38.p12 chr2: 177,973,069-177,983,973 PDE11A
    nsv3876791copy number variation1nstd102humanBenign GRCh37 chr2: 178,838,191-178,848,700 , GRCh38.p12 chr2: 177,973,464-177,983,973 PDE11A
    nsv3870513copy number variation1nstd102humanBenign GRCh37 chr2: 178,845,755-178,849,529 , GRCh38.p12 chr2: 177,981,028-177,984,802 PDE11A
    nsv3877790copy number variation1nstd102humanBenign GRCh37 chr2: 178,844,286-178,847,375 , GRCh38.p12 chr2: 177,979,559-177,982,648 PDE11A
    nsv3888956copy number variation1nstd102humanBenign GRCh37 chr2: 178,856,430-178,857,130 , GRCh38.p12 chr2: 177,991,703-177,992,403 PDE11A
    nsv3886967copy number variation1nstd102humanBenign GRCh37 chr2: 178,740,970-178,741,538 , GRCh38.p12 chr2: 177,876,243-177,876,811 PDE11A
    nsv3876836copy number variation1nstd102humanBenign GRCh37 chr2: 178,777,850-178,836,333 , GRCh38.p12 chr2: 177,913,123-177,971,606 PDE11A
    nsv4454310copy number variation1nstd102humanUncertain significance GRCh37 chr2: 178,683,785-178,697,982 , GRCh38.p12 chr2: 177,819,058-177,833,255 PDE11A
    nsv3875338copy number variation1nstd102humanBenign GRCh37 chr2: 178,833,261-178,862,460 , GRCh38.p12 chr2: 177,968,534-177,997,733 PDE11A, API5P2
    nsv3885120copy number variation1nstd102humanBenign GRCh37 chr2: 178,856,455-178,862,560 , GRCh38.p12 chr2: 177,991,728-177,997,833 PDE11A, API5P2
    nsv3885150copy number variation1nstd102humanBenign GRCh37 chr2: 178,468,493-178,502,353 , GRCh38.p12 chr2: 177,603,765-177,637,625 PDE11A, IFT70A
    nsv3904686copy number variation1nstd102humanLikely benign NCBI36 chr2: 178,258,386-178,285,001 , GRCh37 chr2: 178,550,140-178,576,755 , GRCh38 chr2: 177,685,412-177,712,027 PDE11A, PDE11A-AS1
    nsv3877720copy number variation1nstd102humanBenign GRCh37 chr2: 178,551,924-178,567,474 , GRCh38.p12 chr2: 177,687,196-177,702,746 PDE11A, PDE11A-AS1
    nsv7096361copy number variation1nstd102humanUncertain significance GRCh37 chr2: 178,545,632-178,592,385 , GRCh38.p12 chr2: 177,680,904-177,727,657 PDE11A, PDE11A-AS1
    nsv3900619copy number variation1nstd102humanUncertain significance GRCh37 chr2: 178,550,140-178,585,662 , NCBI36 chr2: 178,258,386-178,293,908 , GRCh38 chr2: 177,685,412-177,720,934 PDE11A, PDE11A-AS1
    nsv3886781copy number variation1nstd102humanUncertain significance GRCh37 chr2: 178,551,957-178,585,662 , GRCh38.p12 chr2: 177,687,229-177,720,934 PDE11A, PDE11A-AS1
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