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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6289911copy number variation2nstd102humanPathogenic GRCh38 chr14: 45,002,867-45,015,056 , GRCh37 chr14: 45,472,063-45,484,252 TOGARAM1
    nsv4728518copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 45,472,062-45,484,253 , GRCh38.p12 chr14: 45,002,859-45,015,050 TOGARAM1
    nsv3898292copy number variation1nstd102humanLikely benign GRCh37 chr14: 45,409,646-45,465,144 , GRCh38.p12 chr14: 44,940,443-44,995,941 TOGARAM1, KLHL28
    nsv6637425copy number variation1nstd102humanUncertain significance GRCh37 chr14: 45,412,511-45,496,926 , GRCh38.p12 chr14: 44,943,308-45,027,723 TOGARAM1, KLHL28
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 TOGARAM1, 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 TOGARAM1, MIR208B, 600 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 TOGARAM1, TTC6, 178 more genes
    nsv3895946copy number variation1nstd102humanPathogenic GRCh37 chr14: 35,934,503-47,120,961 , GRCh38.p12 chr14: 35,465,297-46,651,758 TOGARAM1, PRPF39-DT, 121 more genes
    nsv7094429copy number variation1nstd102humanPathogenic GRCh37 chr14: 44,820,816-45,645,917 , GRCh38.p12 chr14: 44,351,613-45,176,714 TOGARAM1, DOCK11P1, 15 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 TOGARAM1, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 TOGARAM1, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 TOGARAM1, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 TOGARAM1, DHRS7, 1946 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 TOGARAM1, SRMP2, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 TOGARAM1, CRIP1, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 TOGARAM1, MIR656, 1918 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 TOGARAM1, PAPOLA-DT, 1338 more genes
    nsv3913204copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995 TOGARAM1, SMARCE1P3, 635 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 TOGARAM1, CDH24, 623 more genes
    nsv3912538copy number variation1nstd102humanPathogenic GRCh37 chr14: 31,139,520-45,459,798 , GRCh38 chr14: 30,670,314-44,990,595 , NCBI36 chr14: 30,209,271-44,529,548 TOGARAM1, IGBP1P1, 182 more genes
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