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Items: 1 to 20 of 92

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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
    nsv6969579copy number variation1nstd229human GRCh38 chr14: 93,180,060-93,183,832 , GRCh37.p13 chr14: 93,646,405-93,650,177 LYSET, MOAP1
    nsv6968792copy number variation1nstd229human GRCh38 chr14: 93,169,201-93,215,200 , GRCh37.p13 chr14: 93,635,546-93,681,546 MOAP1, GON7, 2 more genes
    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
    nsv6960103copy number variation1nstd229human GRCh38 chr14: 93,110,744-93,186,638 , GRCh37.p13 chr14: 93,577,089-93,652,983 CYB5AP3, ITPK1, 2 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
    nsv6504143copy number variation1nstd223human GRCh38 chr14: 93,184,201-93,186,000 , GRCh37.p13 chr14: 93,650,546-93,652,345 LYSET, MOAP1
    nsv6499962copy number variation1nstd223human GRCh38 chr14: 93,179,113-93,181,391 , GRCh37.p13 chr14: 93,645,458-93,647,736 MOAP1
    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
    nsv5511066copy number variation1nstd206human GRCh38 chr14: 93,180,275-93,181,412 , GRCh37.p13 chr14: 93,646,620-93,647,757 MOAP1
    nsv5506599copy number variation1nstd206human GRCh38 chr14: 92,986,904-93,282,458 , GRCh37.p13 chr14: 93,453,249-93,748,804 BTBD7, RPL18AP1, 8 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
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