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Items: 14

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    Number of Variants: 14

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875047copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483 NEK4, SLMAP, 132 more genes
    nsv3912778copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568 NEK4, SEMA3G, 160 more genes
    nsv4453518copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,195,134-52,869,037 , GRCh38.p12 chr3: 52,161,118-52,835,021 NEK4, SNORD19B, 42 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 NEK4, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NEK4, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 NEK4, RPL23AP49, 2875 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 NEK4, UQCRC1, 291 more genes
    nsv3917135copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 51,406,905-55,073,516 , GRCh37 chr3: 51,431,865-55,098,476 , GRCh38 chr3: 51,394,434-55,064,449 NEK4, ACY1, 96 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 NEK4, DNAH1, 62 more genes
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 NEK4, PHF7, 47 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 NEK4, RRP9, 76 more genes
    nsv6636925copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,780,509-53,418,869 , GRCh38.p12 chr3: 52,746,493-53,384,842 NEK4, LOC105377094, 17 more genes
    nsv6636758copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,783,975-53,418,893 , GRCh38.p12 chr3: 52,749,959-53,384,866 NEK4, MUSTN1, 17 more genes
    nsv3921366copy number variation1nstd102humanUncertain significance NCBI36 chr3: 52,632,666-52,818,082 , GRCh37.p13 chr3: 52,657,626-52,843,042 , GRCh38.p12 chr3: 52,623,610-52,809,026 NEK4, AKTIPP1, 13 more genes
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