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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094433copy number variation1nstd102humanPathogenic GRCh37 chr14: 54,410,919-55,369,403 , GRCh38.p12 chr14: 53,944,201-54,902,685 BMP4, MIR5580, 14 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6953179copy number variation1nstd229human GRCh38 chr14: 54,229,437-54,576,363 , GRCh37.p13 chr14: 54,696,155-55,043,081 CGRRF1, CDKN3, 3 more genes
    nsv6949862copy number variation1nstd229human GRCh38 chr14: 51,123,112-56,995,885 , GRCh37.p13 chr14: 51,589,830-57,462,603 RPL3P3, RNA5SP385, 96 more genes
    nsv6944218copy number variation1nstd229human GRCh38 chr14: 54,396,094-54,423,891 , GRCh37.p13 chr14: 54,862,812-54,890,609 CNIH1, CDKN3
    nsv6943845copy number variation1nstd229human GRCh38 chr14: 54,419,101-54,426,400 , GRCh37.p13 chr14: 54,885,819-54,893,118 CNIH1, CDKN3
    nsv6941647copy number variation1nstd229human GRCh38 chr14: 53,551,791-55,721,697 , GRCh37.p13 chr14: 54,018,509-56,188,415 MIR5580, CDKN3, 40 more genes
    nsv6594668inversion1nstd223human GRCh38 chr14: 54,289,735-54,434,275 , GRCh37.p13 chr14: 54,756,453-54,900,993 CNIH1, CDKN3
    nsv6587212inversion1nstd223human GRCh38 chr14: 54,421,278-54,422,258 , GRCh37.p13 chr14: 54,887,996-54,888,976 CNIH1
    nsv6578746inversion1nstd223human GRCh38 chr14: 49,838,941-56,572,992 , GRCh37.p13 chr14: 50,305,659-57,039,710 LOC100419913, TXNDC16, 124 more genes
    nsv6488051copy number variation1nstd223human GRCh38 chr14: 54,427,341-54,427,837 , GRCh37.p13 chr14: 54,894,059-54,894,555 CNIH1
    nsv6487218copy number variation1nstd223human GRCh38 chr14: 54,437,701-54,443,500 , GRCh37.p13 chr14: 54,904,419-54,910,218 CNIH1
    nsv6481581copy number variation1nstd223human GRCh38 chr14: 54,438,001-54,446,800 , GRCh37.p13 chr14: 54,904,719-54,913,518 CNIH1
    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
    nsv6314214copy number variation1nstd102humanPathogenic GRCh37 chr14: 53,241,194-55,803,026 , GRCh38.p12 chr14: 52,774,476-55,336,308 RPL34P28, MIR5580, 41 more genes
    nsv6309696copy number variation1nstd102humanPathogenic GRCh37 chr14: 54,416,750-55,369,403 , GRCh38.p12 chr14: 53,950,032-54,902,685 MIR4308, FDPSP3, 13 more genes
    nsv6188697copy number variation1nstd214human GRCh38 chr14: 54,441,113-54,441,166 , GRCh37.p13 chr14: 54,907,831-54,907,884 CNIH1
    nsv6133131copy number variation1nstd213human GRCh37 chr14: 52,470,000-55,150,001 , GRCh38.p12 chr14: 52,003,282-54,683,283 PSMC6, PTGER2, 35 more genes
    nsv6081655insertion1nstd212human GRCh38 chr14: 54,426,477-54,426,477 , GRCh37.p13 chr14: 54,893,195-54,893,195 CNIH1
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