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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5508523copy number variation1nstd206human GRCh38 chr14: 21,154,165-21,156,072 , GRCh37.p13 chr14: 21,622,324-21,624,231 OR5AU1
    nsv5497719copy number variation1nstd206human GRCh38 chr14: 21,150,209-21,164,360 , GRCh37.p13 chr14: 21,618,368-21,632,519 OR5AU1, SMARCE1P3
    nsv5374430translocation1nstd200human GRCh38 chr14: 21,155,967-21,155,967 , GRCh38 chr14: 21,154,273-21,154,273 , GRCh37.p13 chr14: 21,624,126-21,624,126 , GRCh37.p13 chr14: 21,622,432-21,622,432 OR5AU1
    nsv4994085copy number variation1nstd200human GRCh38 chr14: 21,145,708-21,193,069 , GRCh37.p13 chr14: 21,613,867-21,661,228 OR5AU1, SMARCE1P3, 1 more genes
    nsv4994083copy number variation1nstd200human GRCh38 chr14: 21,119,677-21,207,571 , GRCh37.p13 chr14: 21,587,836-21,675,730 HNRNPC, LOC105378175, 5 more genes
    nsv4990739copy number variation1nstd200human GRCh38 chr14: 21,125,664-21,153,769 , GRCh37.p13 chr14: 21,593,823-21,621,928 LOC105378175, OR5AU1
    nsv4835705copy number variation1nstd200human GRCh37 chr14: 21,622,403-21,624,130 , GRCh38.p12 chr14: 21,154,244-21,155,971 OR5AU1
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 more genes
    nsv4675976copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,589,998-21,999,445 , GRCh38.p12 chr14: 21,121,839-21,531,311 LOC105378175, SUPT16H, 19 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4668562copy number variation1nstd186human GRCh37 chr14: 21,622,388-21,624,197 , GRCh38.p12 chr14: 21,154,229-21,156,038 OR5AU1
    nsv4630250copy number variation1nstd183human GRCh37 chr14: 21,622,944-21,624,197 , GRCh38.p12 chr14: 21,154,785-21,156,038 OR5AU1
    nsv4629644copy number variation1nstd183human GRCh37 chr14: 21,496,021-21,671,277 , GRCh38.p12 chr14: 21,027,862-21,203,118 RNASE13, RNU6-252P, 15 more genes
    nsv4625871copy number variation1nstd183human GRCh37 chr14: 21,606,520-21,651,176 , GRCh38.p12 chr14: 21,138,361-21,183,017 LOC100129923, OR5AU1, 1 more genes
    nsv4622942copy number variation1nstd183human GRCh37 chr14: 21,622,388-21,624,197 , GRCh38.p12 chr14: 21,154,229-21,156,038 OR5AU1
    nsv4621176copy number variation1nstd183human GRCh37 chr14: 21,606,520-21,713,173 , GRCh38.p12 chr14: 21,138,361-21,245,014 OR5AU1, SMARCE1P3, 3 more genes
    nsv4620068copy number variation1nstd183human GRCh37 chr14: 21,622,842-21,624,160 , GRCh38.p12 chr14: 21,154,683-21,156,001 OR5AU1
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