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Items: 1 to 20 of 125

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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
    nsv7076778inversion1nstd229human GRCh38 chr14: 92,926,422-92,926,434 , GRCh37.p13 chr14: 93,392,767-93,392,779 CHGA
    nsv7073028inversion1nstd229human GRCh38 chr14: 92,780,313-93,169,180 , GRCh37.p13 chr14: 93,351,784-93,635,525 CYB5AP3, GOLGA5, 5 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
    nsv6977955copy number variation1nstd229human GRCh38 chr14: 92,787,466-92,928,485 , GRCh37.p13 chr14: 93,253,811-93,372,264 GOLGA5, LINC02287, 2 more genes
    nsv6974600copy number variation1nstd229human GRCh38 chr14: 92,929,294-92,929,374 , GRCh37.p13 chr14: 93,395,639-93,395,719 CHGA
    nsv6964194copy number variation1nstd229human GRCh38 chr14: 92,932,640-93,474,765 , GRCh37.p13 chr14: 93,398,985-93,941,111 UNC79, UBR7, 12 more genes
    nsv6958758copy number variation1nstd229human GRCh38 chr14: 92,925,956-92,970,921 , GRCh37.p13 chr14: 93,392,301-93,437,266 CHGA, ITPK1
    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
    nsv6187968copy number variation1nstd214human GRCh38 chr14: 92,929,294-92,929,373 , GRCh37.p13 chr14: 93,395,639-93,395,718 CHGA
    nsv5928539copy number variation1nstd209human GRCh38 chr14: 92,929,294-92,929,373 , GRCh37.p13 chr14: 93,395,639-93,395,718 CHGA
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