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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3871907copy number variation1nstd102humanBenign GRCh37 chr3: 58,728,125-58,806,556 , GRCh38.p12 chr3: 58,742,398-58,820,830 CFAP20DC
    nsv3886616copy number variation1nstd102humanBenign GRCh37 chr3: 58,782,604-58,807,458 , GRCh38.p12 chr3: 58,796,877-58,821,732 CFAP20DC
    nsv3873801copy number variation1nstd102humanBenign GRCh37 chr3: 58,789,803-58,807,458 , GRCh38.p12 chr3: 58,804,077-58,821,732 CFAP20DC
    nsv3872688copy number variation1nstd102humanBenign GRCh37 chr3: 58,798,468-58,807,458 , GRCh38.p12 chr3: 58,812,742-58,821,732 CFAP20DC
    nsv3888018copy number variation1nstd102humanBenign GRCh37 chr3: 58,798,468-58,806,556 , GRCh38.p12 chr3: 58,812,742-58,820,830 CFAP20DC
    nsv3876178copy number variation1nstd102humanBenign GRCh37 chr3: 58,798,468-58,804,998 , GRCh38.p12 chr3: 58,812,742-58,819,272 CFAP20DC
    nsv3879582copy number variation1nstd102humanBenign GRCh37 chr3: 58,798,468-58,804,178 , GRCh38.p12 chr3: 58,812,742-58,818,452 CFAP20DC
    nsv3879149copy number variation1nstd102humanBenign GRCh37 chr3: 59,697,659-59,700,279 , GRCh38.p12 chr3: 59,711,933-59,714,553 CFAP20DC-DT
    nsv3880268copy number variation1nstd102humanBenign GRCh37 chr3: 58,798,468-58,800,898 , GRCh38.p12 chr3: 58,812,742-58,815,172 CFAP20DC
    nsv3879700copy number variation1nstd102humanBenign GRCh37 chr3: 59,739,919-59,820,558 , GRCh38.p12 chr3: 59,754,193-59,834,832 CFAP20DC-DT, FHIT
    nsv3879110copy number variation1nstd102humanBenign GRCh37 chr3: 58,798,468-58,823,639 , GRCh38.p12 chr3: 58,812,742-58,837,913 CFAP20DC, CFAP20DC-AS1
    nsv4728569copy number variation1nstd102humanUncertain significance GRCh37 chr3: 58,757,175-58,934,036 , GRCh38.p12 chr3: 58,771,448-58,948,310 CFAP20DC, CFAP20DC-AS1
    nsv3921706copy number variation1nstd102humanUncertain significance NCBI36 chr3: 58,830,999-59,581,504 , GRCh37 chr3: 58,855,959-59,606,464 , GRCh38 chr3: 58,870,233-59,620,738 CFAP20DC, SNRPB2P1, 2 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 CFAP20DC, LOC105377171, 323 more genes
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 CFAP20DC, MAGI1-AS1, 135 more genes
    nsv6290933copy number variation1nstd102humanPathogenic GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004 NDUFB4P1, UBA3, 110 more genes
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 CFAP20DC, LOC105377114, 110 more genes
    nsv3875047copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483 CFAP20DC, SLMAP, 132 more genes
    nsv3917204copy number variation1nstd102humanPathogenic GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197 CFAP20DC, C3orf49, 93 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CFAP20DC, RNU4-62P, 2880 more genes
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