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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
    nsv7066512inversion1nstd229human GRCh38 chr14: 92,024,779-92,024,841 , GRCh37.p13 chr14: 92,491,123-92,491,185 PTMAP7, TRIP11
    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
    nsv6970667copy number variation1nstd229human GRCh38 chr14: 92,022,185-92,109,534 , GRCh37.p13 chr14: 92,488,529-92,575,878 TRIP11, ATXN3, 1 more genes
    nsv6958450copy number variation1nstd229human GRCh38 chr14: 91,991,801-92,160,300 , GRCh37.p13 chr14: 92,458,145-92,626,644 PTMAP7, TRIP11, 3 more genes
    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
    nsv6591551inversion1nstd223human GRCh38 chr14: 91,074,052-93,300,799 , GRCh37.p13 chr14: 91,540,396-93,674,575 LINC02287, LGMN, 39 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
    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
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5004934copy number variation1nstd200human GRCh38 chr14: 91,569,497-92,338,399 , GRCh37.p13 chr14: 92,073,684-92,804,743 LOC101928957, FBLN5, 13 more genes
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