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Items: 1 to 20 of 88

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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
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv7058992inversion1nstd229human GRCh38 chr14: 90,104,468-93,174,563 , GRCh37.p13 chr14: 90,570,812-93,372,264 LINC02321, TC2N, 48 more genes
    nsv6959209copy number variation1nstd229human GRCh38 chr14: 90,676,901-90,708,200 , GRCh37.p13 chr14: 91,143,245-91,174,544 LOC105370622, TTC7B
    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
    nsv6576886inversion1nstd223human GRCh38 chr14: 87,626,564-93,230,084 , GRCh37.p13 chr14: 88,092,908-93,674,575 ATXN3, RIN3, 87 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
    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
    nsv6133140copy number variation1nstd213human GRCh37 chr14: 90,990,000-93,500,001 , GRCh38.p12 chr14: 90,523,656-92,905,919 ATXN3, GPR68, 34 more genes
    nsv6121213copy number variation1nstd186human GRCh37 chr14: 91,161,242-91,161,708 , GRCh38.p12 chr14: 90,694,898-90,695,364 LOC105370622, TTC7B
    nsv6030303copy number variation1nstd212human GRCh38 chr14: 90,694,657-92,547,405 , GRCh37.p13 chr14: 91,161,001-93,013,750 , PTMAP7, 30 more genes
    nsv6024293copy number variation1nstd212human GRCh38 chr14: 90,695,157-92,546,976 , GRCh37.p13 chr14: 91,161,501-93,013,321 , NANOGP7, 30 more genes
    nsv5698987mobile element insertion2nstd211human GRCh38 chr14: 90,695,868-90,695,868 , GRCh37.p13 chr14: 91,162,212-91,162,212 TTC7B, LOC105370622
    nsv5647819insertion1nstd207human GRCh38 chr14: 90,695,851-90,695,851 , GRCh37.p13 chr14: 91,162,195-91,162,195 LOC105370622, TTC7B
    nsv5499002copy number variation1nstd206human GRCh38 chr14: 90,694,898-90,695,364 , GRCh37.p13 chr14: 91,161,242-91,161,708 LOC105370622, TTC7B
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
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