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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096091copy number variation1nstd102humanPathogenic GRCh37 chr21: 19,775,775-19,775,939 , GRCh38.p12 chr21: 18,403,458-18,403,622 TMPRSS15
    nsv7096090copy number variation1nstd102humanUncertain significance GRCh37 chr21: 19,642,286-19,775,939 , GRCh38.p12 chr21: 18,269,969-18,403,622 TMPRSS15
    nsv4457688copy number variation1nstd102humanUncertain significance GRCh37 chr21: 19,721,193-19,802,272 , GRCh38.p12 chr21: 18,348,876-18,429,955 TMPRSS15
    nsv7096277copy number variation1nstd102humanUncertain significance GRCh37 chr21: 19,704,381-19,716,397 , GRCh38.p12 chr21: 18,332,064-18,344,080 TMPRSS15
    nsv3899646copy number variation1nstd102humanLikely benign GRCh37 chr21: 19,622,822-19,810,737 , GRCh38.p12 chr21: 18,250,505-18,438,420 TMPRSS15, CHODL
    nsv4676356copy number variation1nstd102humanUncertain significance GRCh37 chr21: 19,325,631-20,044,818 , GRCh38.p12 chr21: 17,953,314-18,672,500 TMPRSS15, CHODL, 1 more genes
    nsv3923176copy number variation1nstd102humanPathogenic GRCh38 chr21: 7,817,158-46,670,440 , NCBI36 chr21: 14,406,909-46,914,780 , GRCh37 chr21: 15,485,038-48,090,352 TMPRSS15, COL18A1-AS2, 682 more genes
    nsv3905423copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,538,655-48,080,926 , GRCh38.p12 chr21: 14,166,334-46,661,014 TMPRSS15, MTND5P1, 581 more genes
    nsv3917693copy number variation1nstd102humanPathogenic GRCh38 chr21: 7,749,532-37,653,653 , GRCh37 chr21: 15,451,032-39,025,955 , NCBI36 chr21: 14,372,903-37,947,825 TMPRSS15, DPRXP5, 448 more genes
    nsv3922838copy number variation1nstd102humanPathogenic GRCh38 chr21: 10,366,915-27,611,416 , GRCh37.p13 chr21: 14,338,130-28,983,735 TMPRSS15, RN7SL163P, 178 more genes
    nsv3916181copy number variation1nstd102humanPathogenic GRCh38 chr21: 14,000,720-30,903,065 , GRCh37 chr21: 15,373,041-32,275,384 , NCBI36 chr21: 14,294,912-31,197,255 TMPRSS15, ADAMTS5, 215 more genes
    nsv3920431copy number variation1nstd102humanPathogenic NCBI36 chr21: 13,488,537-29,551,400 , GRCh37 chr21: 14,566,666-30,629,529 , GRCh38 chr21: 13,194,345-29,257,208 TMPRSS15, ZNF114P1, 189 more genes
    nsv4676306copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,325,923 , GRCh38.p12 chr21: 13,634,136-27,953,605 TMPRSS15, JAM2, 161 more genes
    nsv3921072copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,458-29,235,160 , GRCh38 chr21: 13,634,137-27,862,841 , NCBI36 chr21: 13,928,329-28,157,031 TMPRSS15, CYYR1-AS1, 161 more genes
    nsv3909006copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,225,300 , GRCh38.p12 chr21: 13,634,136-27,852,981 TMPRSS15, LOC105372738, 161 more genes
    nsv3917277copy number variation1nstd102humanPathogenic GRCh38 chr21: 13,974,874-27,814,120 , GRCh37.p13 chr21: 15,347,195-29,186,439 TMPRSS15, SREK1IP1P1, 141 more genes
    nsv3897353copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-25,292,671 , GRCh38.p12 chr21: 13,634,136-23,920,355 TMPRSS15, LOC105372740, 117 more genes
    nsv4676170copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-24,522,577 , GRCh38.p12 chr21: 13,634,136-23,150,255 TMPRSS15, FDPSP6, 108 more genes
    nsv3921594copy number variation1nstd102humanPathogenic NCBI36 chr21: 15,635,906-23,120,507 , GRCh38 chr21: 15,341,716-22,826,315 , GRCh37 chr21: 16,714,035-24,198,636 TMPRSS15, VDAC2P1, 62 more genes
    nsv3914189copy number variation1nstd102humanPathogenic NCBI36 chr21: 14,406,909-21,591,464 , GRCh38 chr21: 14,112,717-21,297,273 , GRCh37 chr21: 15,485,038-22,669,593 TMPRSS15, GAPDHP16, 69 more genes
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