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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148135copy number variation1nstd102humanUncertain significance GRCh37 chr14: 57,675,327-59,806,898 , GRCh38.p12 chr14: 57,208,609-59,340,180 HMGB1P14, TOMM20L-DT, 36 more genes
    nsv7072847inversion1nstd229human GRCh38 chr14: 57,371,756-57,740,063 , GRCh37.p13 chr14: 57,838,474-58,206,781 LOC401777, LOC105370519, 4 more genes
    nsv7060471inversion1nstd229human GRCh38 chr14: 54,671,401-63,742,041 , GRCh37.p13 chr14: 55,138,119-64,208,759 KTN1, OTX2-AS1, 153 more genes
    nsv6952443copy number variation1nstd229human GRCh38 chr14: 57,104,906-61,096,631 , GRCh37.p13 chr14: 57,571,624-61,563,349 LRRC9, RTN1, 71 more genes
    nsv6949011copy number variation1nstd229human GRCh38 chr14: 57,104,849-61,096,728 , GRCh37.p13 chr14: 57,571,567-61,563,446 MAD2L1P1, AP5M1, 71 more genes
    nsv6944214copy number variation1nstd229human GRCh38 chr14: 57,377,661-57,392,297 , GRCh37.p13 chr14: 57,844,379-57,859,015 NAA30
    nsv6943920copy number variation1nstd229human GRCh38 chr14: 57,187,604-57,469,829 , GRCh37.p13 chr14: 57,654,322-57,936,547 CCDC198, EXOC5, 2 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 PARP1P2, HIF1A, 91 more genes
    nsv6622787copy number variation1nstd224human GRCh37 chr14: 57,287,812-59,826,703 , GRCh38.p12 chr14: 56,821,094-59,359,985 KIAA0586, DAAM1, 41 more genes
    nsv6594267inversion1nstd223human GRCh38 chr14: 54,883,431-63,921,497 , GRCh37.p13 chr14: 55,350,149-64,388,215 RPL36AP1, GNRHR2P1, 152 more genes
    nsv6493736copy number variation1nstd223human GRCh38 chr14: 57,203,867-58,132,081 , GRCh37.p13 chr14: 57,670,585-58,598,799 LOC401777, EXOC5, 9 more genes
    nsv6481328copy number variation1nstd223human GRCh38 chr14: 57,377,661-57,392,297 , GRCh37.p13 chr14: 57,844,379-57,859,015 NAA30
    nsv6478981copy number variation1nstd223human GRCh38 chr14: 57,387,001-57,388,700 , GRCh37.p13 chr14: 57,853,719-57,855,418 NAA30
    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
    nsv6132789copy number variation1nstd213human GRCh37 chr14: 56,650,000-58,500,001 , GRCh38.p12 chr14: 56,183,282-58,033,283 TMEM260, CCDC198, 19 more genes
    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
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5700308mobile element insertion1nstd211human GRCh38 chr14: 57,400,732-57,400,732 , GRCh37.p13 chr14: 57,867,450-57,867,450 NAA30
    nsv5511999copy number variation1nstd206human GRCh38 chr14: 57,401,522-57,401,924 , GRCh37.p13 chr14: 57,868,240-57,868,642 NAA30
    nsv5415322mobile element insertion1nstd206human GRCh38 chr14: 57,400,732-57,400,783 , GRCh37.p13 chr14: 57,867,450-57,867,501 NAA30
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