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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3876802copy number variation1nstd102humanBenign GRCh37 chr3: 131,989,621-132,012,079 , GRCh38.p12 chr3: 132,270,777-132,293,235 CPNE4
    nsv3879518copy number variation1nstd102humanBenign GRCh37 chr3: 131,984,573-131,993,582 , GRCh38.p12 chr3: 132,265,729-132,274,738 CPNE4
    nsv3883865copy number variation1nstd102humanBenign GRCh37 chr3: 131,708,352-131,716,105 , GRCh38.p12 chr3: 131,989,508-131,997,261 CPNE4
    nsv3883627copy number variation1nstd102humanBenign GRCh37 chr3: 131,672,688-131,673,311 , GRCh38.p12 chr3: 131,953,844-131,954,467 CPNE4
    nsv3877895copy number variation1nstd102humanBenign GRCh37 chr3: 131,673,111-131,673,311 , GRCh38.p12 chr3: 131,954,267-131,954,467 CPNE4
    nsv3880615copy number variation1nstd102humanBenign GRCh37 chr3: 131,690,374-131,713,326 , GRCh38.p12 chr3: 131,971,530-131,994,482 CPNE4, MIR5704
    nsv3885466copy number variation1nstd102humanBenign GRCh37 chr3: 131,690,374-131,713,017 , GRCh38.p12 chr3: 131,971,530-131,994,173 CPNE4, MIR5704
    nsv3886396copy number variation1nstd102humanBenign GRCh37 chr3: 131,696,103-131,713,566 , GRCh38.p12 chr3: 131,977,259-131,994,722 CPNE4, MIR5704
    nsv4674665copy number variation1nstd102humanLikely benign GRCh37 chr3: 131,649,934-131,884,654 , GRCh38.p12 chr3: 131,931,090-132,165,810 CPNE4, LOC105374111, 1 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 CPNE4, NPHP3-AS1, 218 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 CPNE4, HNRNPA1P23, 278 more genes
    nsv3914757copy number variation1nstd102humanPathogenic NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997 CPNE4, CLSTN2-AS1, 177 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 CPNE4, RNU6-789P, 169 more genes
    nsv3918871copy number variation1nstd102humanPathogenic GRCh38 chr3: 130,401,265-139,005,019 , NCBI36 chr3: 131,602,799-140,206,551 , GRCh37 chr3: 130,120,109-138,723,861 CPNE4, FOXL2, 132 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CPNE4, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 CPNE4, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 CPNE4, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 CPNE4, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 CPNE4, H1-10, 846 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 CPNE4, OR7E53P, 794 more genes
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