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Items: 1 to 20 of 78

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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
    nsv7061775inversion1nstd229human GRCh38 chr14: 94,128,659-94,128,764 , GRCh37.p13 chr14: 94,594,996-94,595,101 IFI27L2
    nsv6960583copy number variation1nstd229human GRCh38 chr14: 94,125,080-94,127,670 , GRCh37.p13 chr14: 94,591,417-94,594,007 IFI27L2
    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
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 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
    nsv6314100copy number variation1nstd102humanUncertain significance GRCh37 chr14: 94,400,492-96,192,218 , GRCh38.p12 chr14: 94,115,593-95,725,881 DICER1, LOC105370634, 45 more genes
    nsv6309604copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 93,687,728-95,560,403 , GRCh38.p12 chr14: 93,638,887-95,094,066 , GRCh38.p12 chr14|NT_187601.1: 335,944-1,475,710 SERPINA3, SERPINA6, 43 more genes
    nsv6132940copy number variation1nstd213human GRCh37 chr14: 93,690,000-95,350,001 , GRCh38.p12 chr14: 93,638,887-94,883,664 , GRCh38.p12 chr14|NT_187601.1: 338,216-1,475,710 SERPINA3, ASB2, 40 more genes
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4322697inversion1nstd166human GRCh37.p13 chr14: 93,328,296-94,706,279 , GRCh38.p12 chr14: 92,861,951-94,140,555 , GRCh38.p12 chr14|NT_187601.1: 1-1,354,504 ASB2, UNC79, 29 more genes
    nsv4226368copy number variation1nstd166human GRCh37.p13 chr14: 94,596,251-94,596,434 , GRCh38.p12 chr14: 94,129,914-94,130,097 , GRCh38.p12 chr14|NT_187601.1: 1,244,476-1,244,659 IFI27L2
    nsv3922566copy number variation1nstd102humanPathogenic GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786 RPSAP4, LOC105370622, 97 more genes
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