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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6975081copy number variation1nstd229human GRCh38 chr14: 75,145,638-75,149,199 , GRCh37.p13 chr14: 75,612,341-75,615,902 TMED10
    nsv6974859copy number variation1nstd229human GRCh38 chr14: 75,161,536-75,168,585 , GRCh37.p13 chr14: 75,628,239-75,635,288 TMED10
    nsv6974125copy number variation1nstd229human GRCh38 chr14: 75,150,054-75,150,518 , GRCh37.p13 chr14: 75,616,757-75,617,221 TMED10
    nsv6972922copy number variation1nstd229human GRCh38 chr14: 75,150,020-75,150,489 , GRCh37.p13 chr14: 75,616,723-75,617,192 TMED10
    nsv6967574copy number variation1nstd229human GRCh38 chr14: 75,169,301-75,380,900 , GRCh37.p13 chr14: 75,636,004-75,847,603 DPPA5P4, TMED10, 3 more genes
    nsv6958392copy number variation1nstd229human GRCh38 chr14: 75,156,667-75,160,810 , GRCh37.p13 chr14: 75,623,370-75,627,513 TMED10
    nsv6593668inversion1nstd223human GRCh38 chr14: 75,135,286-75,136,159 , GRCh37.p13 chr14: 75,601,989-75,602,862 TMED10
    nsv6590523inversion1nstd223human GRCh38 chr14: 75,153,732-75,154,399 , GRCh37.p13 chr14: 75,620,435-75,621,102 TMED10
    nsv6582899inversion1nstd223human GRCh38 chr14: 75,143,088-75,143,757 , GRCh37.p13 chr14: 75,609,791-75,610,460 TMED10
    nsv6580993inversion1nstd223human GRCh38 chr14: 75,140,145-75,140,542 , GRCh37.p13 chr14: 75,606,848-75,607,245 TMED10
    nsv6579415inversion1nstd223human GRCh38 chr14: 75,163,125-75,163,934 , GRCh37.p13 chr14: 75,629,828-75,630,637 TMED10
    nsv6576386inversion1nstd223human GRCh38 chr14: 75,137,173-75,137,838 , GRCh37.p13 chr14: 75,603,876-75,604,541 TMED10
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6273755copy number variation1nstd214human GRCh38 chr14: 75,132,273-75,132,349 , GRCh37.p13 chr14: 75,598,976-75,599,052 TMED10
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5505203copy number variation1nstd206human GRCh38 chr14: 75,152,859-75,196,873 , GRCh37.p13 chr14: 75,619,562-75,663,576 TMED10
    nsv5501011copy number variation1nstd206human GRCh38 chr14: 75,132,275-75,132,350 , GRCh37.p13 chr14: 75,598,978-75,599,053 TMED10
    nsv5500841copy number variation1nstd206human GRCh38 chr14: 75,140,282-75,142,991 , GRCh37.p13 chr14: 75,606,985-75,609,694 TMED10
    nsv5155397mobile element insertion1nstd203human GRCh38 chr14: 75,164,546-75,164,552 , GRCh37.p13 chr14: 75,631,249-75,631,255 TMED10
    nsv5148580mobile element insertion1nstd203human GRCh38 chr14: 75,133,734-75,133,749 , GRCh37.p13 chr14: 75,600,437-75,600,452 TMED10
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