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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3890258copy number variation1nstd102humanBenign GRCh37 chr21: 19,161,515-19,171,547 , GRCh38.p12 chr21: 17,789,198-17,799,230 C21orf91-OT1, C21orf91
    nsv6637699copy number variation1nstd102humanUncertain significance GRCh37 chr21: 18,965,618-19,018,155 , GRCh38.p12 chr21|NT_187627.1: 1-42,143 , GRCh38.p12 chr21: 17,593,300-17,645,837 BTG3, CXADR, 1 more genes
    nsv6637579copy number variation1nstd102humanUncertain significance GRCh37 chr21: 19,139,329-19,613,840 , GRCh38.p12 chr21: 17,767,012-18,241,523 CHODL-AS1, C21orf91-OT1, 3 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 BTG3, 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 BTG3, 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 BTG3, DPRXP5, 448 more genes
    nsv3922838copy number variation1nstd102humanPathogenic GRCh38 chr21: 10,366,915-27,611,416 , GRCh37.p13 chr21: 14,338,130-28,983,735 BTG3, 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 BTG3, 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 BTG3, ZNF114P1, 189 more genes
    nsv4676306copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,325,923 , GRCh38.p12 chr21: 13,634,136-27,953,605 BTG3, 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 BTG3, 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 BTG3, LOC105372738, 161 more genes
    nsv3917277copy number variation1nstd102humanPathogenic GRCh38 chr21: 13,974,874-27,814,120 , GRCh37.p13 chr21: 15,347,195-29,186,439 BTG3, SREK1IP1P1, 141 more genes
    nsv3897353copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-25,292,671 , GRCh38.p12 chr21: 13,634,136-23,920,355 BTG3, LOC105372740, 117 more genes
    nsv4676170copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-24,522,577 , GRCh38.p12 chr21: 13,634,136-23,150,255 BTG3, 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 BTG3, 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 BTG3, GAPDHP16, 69 more genes
    nsv3911400copy number variation1nstd102humanPathogenic GRCh38 chr21: 14,127,526-19,238,720 , GRCh37 chr21: 15,499,847-20,611,037 , NCBI36 chr21: 14,421,718-19,532,908 BTG3, RPL39P40, 52 more genes
    nsv3914745copy number variation1nstd102humanPathogenic GRCh38 chr21: 13,634,136-18,211,199 , GRCh37 chr21: 15,006,457-19,583,516 , NCBI36 chr21: 13,928,328-18,505,387 BTG3, LOC105372738, 74 more genes
    nsv3919632copy number variation1nstd102humanPathogenic NCBI36 chr21: 14,314,039-18,419,240 , GRCh37 chr21: 15,392,168-19,497,369 , GRCh38 chr21: 14,019,847-18,125,051 BTG3, RPL39P40, 51 more genes
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