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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    nsv7094351copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-97,347,545 , GRCh38.p12 chr14: 89,963,115-96,881,208 FBLN5, CYB5AP3, 135 more genes
    nsv7094350copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-94,856,914 , GRCh38.p12 chr14: 89,963,115-94,390,577 LOC105370619, SLC24A4, 78 more genes
    nsv6978002copy number variation1nstd229human GRCh38 chr14: 93,933,890-93,934,254 , GRCh37.p13 chr14: 94,400,236-94,400,600 ASB2
    nsv6977546copy number variation1nstd229human GRCh38 chr14: 93,947,922-94,028,320 , GRCh37.p13 chr14: 94,414,268-94,494,666 CCDC197, LOC107984663, 3 more genes
    nsv6976970copy number variation1nstd229human GRCh38 chr14: 93,933,470-93,940,429 , GRCh37.p13 chr14: 94,399,816-94,406,775 ASB2
    nsv6976533copy number variation1nstd229human GRCh38 chr14: 93,947,201-93,947,612 , GRCh37.p13 chr14: 94,413,547-94,413,958 ASB2, MIR4506
    nsv6974818copy number variation1nstd229human GRCh38 chr14: 93,689,101-94,054,300 , GRCh37.p13 chr14: 94,155,447-94,520,646 CCDC197, DDX24, 9 more genes
    nsv6971793copy number variation1nstd229human GRCh38 chr14: 93,932,168-93,936,401 , GRCh37.p13 chr14: 94,398,514-94,402,747 ASB2
    nsv6967999copy number variation1nstd229human GRCh38 chr14: 93,948,638-93,948,735 , GRCh37.p13 chr14: 94,414,984-94,415,081 MIR4506, ASB2
    nsv6966632copy number variation1nstd229human GRCh38 chr14: 93,937,112-93,958,644 , GRCh37.p13 chr14: 94,403,458-94,424,990 ASB2, MIR4506
    nsv6960955copy number variation1nstd229human GRCh38 chr14: 93,930,653-93,934,059 , GRCh37.p13 chr14: 94,396,999-94,400,405 ASB2
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6622585copy number variation1nstd224human GRCh37 chr14: 94,417,390-94,485,954 , GRCh38.p12 chr14: 93,951,044-94,019,608 , GRCh38.p12 chr14|NT_187601.1: 1,065,606-1,134,170 ASB2, CCDC197, 1 more genes
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 more genes
    nsv6514661copy number variation1nstd223human GRCh38 chr14: 93,947,922-94,028,320 , GRCh37.p13 chr14: 94,414,268-94,494,666 ASB2, OTUB2, 3 more genes
    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
    nsv6314210copy number variation1nstd102humanUncertain significance GRCh37 chr14: 94,442,454-95,185,710 , GRCh38.p12 chr14|NT_187601.1: 1,090,670-1,475,710 , GRCh38.p12 chr14: 94,115,593-94,719,373 LOC105370635, IFI27, 23 more genes
    nsv6314190copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,345,625-94,773,741 , GRCh38.p12 chr14: 87,879,281-94,140,555 EML5, LOC105370612, 104 more genes
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