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Items: 1 to 20 of 36

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909113copy number variation1nstd102humanBenign GRCh37 chr14: 39,762,575-39,866,823 , GRCh38.p12 chr14: 39,293,371-39,397,619 FBXO33, MIA2, 1 more genes
    nsv4676064copy number variation1nstd102humanUncertain significance GRCh37 chr14: 39,876,467-40,091,340 , GRCh38.p12 chr14: 39,407,263-39,622,136 FBXO33, LOC105370461, 2 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 FBXO33, HNRNPC, 616 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 FBXO33, MIR208B, 600 more genes
    nsv3917157copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355 FBXO33, LINC02300, 274 more genes
    nsv3916173copy number variation1nstd102humanPathogenic NCBI36 chr14: 33,118,898-48,418,573 , GRCh37.p13 chr14: 34,049,147-49,348,823 , GRCh38.p12 chr14: 33,579,941-48,879,620 FBXO33, TTC6, 178 more genes
    nsv3924751copy number variation1nstd102humanPathogenic GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084 FBXO33, DNAJC8P1, 171 more genes
    nsv3895946copy number variation1nstd102humanPathogenic GRCh37 chr14: 35,934,503-47,120,961 , GRCh38.p12 chr14: 35,465,297-46,651,758 FBXO33, PRPF39-DT, 121 more genes
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 FBXO33, RPLP0P3, 131 more genes
    nsv3921024copy number variation1nstd102humanPathogenic GRCh37 chr14: 35,537,482-44,463,980 , GRCh38 chr14: 35,068,276-43,994,777 , NCBI36 chr14: 34,607,233-43,533,730 FBXO33, LOC107984681, 101 more genes
    nsv3912278copy number variation1nstd102humanPathogenic GRCh38 chr14: 33,880,412-42,359,485 , NCBI36 chr14: 33,419,369-41,898,438 , GRCh37 chr14: 34,349,618-42,828,688 FBXO33, RPL23AP8, 120 more genes
    nsv4676032copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,830,396-42,541,277 , GRCh38.p12 chr14: 36,361,190-42,072,074 FBXO33, PPIAP4, 60 more genes
    nsv6313916copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,862,276-41,597,549 , GRCh38.p12 chr14: 36,393,071-41,128,344 FBXO33, LOC105370462, 55 more genes
    nsv3921621copy number variation1nstd102humanPathogenic GRCh38 chr14: 36,434,568-41,102,476 , GRCh37 chr14: 36,903,773-41,571,681 , NCBI36 chr14: 35,973,524-40,641,431 FBXO33, CLEC14A, 54 more genes
    nsv3891331copy number variation1nstd102humanPathogenic GRCh37 chr14: 35,850,213-40,138,562 , GRCh38.p12 chr14: 35,381,007-39,669,358 FBXO33, LOC105370452, 70 more genes
    nsv3915052copy number variation1nstd102humanPathogenic NCBI36 chr14: 38,356,772-40,433,345 , GRCh38 chr14: 38,817,817-40,894,390 , GRCh37 chr14: 39,287,021-41,363,595 FBXO33, MIA2-AS1, 25 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 FBXO33, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 FBXO33, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 FBXO33, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 FBXO33, DHRS7, 1946 more genes
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