ClinVar

GRCh37/hg19 19q13.12(chr19:35658728-36173537)x3

Genes:

• ATP4A:ATPase H+/K+ transporting subunit alpha [Gene - OMIM - HGNC]
• CD22:CD22 molecule [Gene - OMIM - HGNC]
• ETV2:ETS variant transcription factor 2 [Gene - OMIM - HGNC]
• FXYD5:FXYD domain containing ion transport regulator 5 [Gene - OMIM - HGNC]
• GPR42:G protein-coupled receptor 42 [Gene - OMIM - HGNC]
• HAUS5:HAUS augmin like complex subunit 5 [Gene - OMIM - HGNC]
• RBM42:RNA binding motif protein 42 [Gene - OMIM - HGNC]
• COX6B1:cytochrome c oxidase subunit 6B1 [Gene - OMIM - HGNC]
• DMKN:dermokine [Gene - OMIM - HGNC]
• FAM187B:family with sequence similarity 187 member B [Gene - HGNC]
• FFAR1:free fatty acid receptor 1 [Gene - OMIM - HGNC]
• FFAR2:free fatty acid receptor 2 [Gene - OMIM - HGNC]
• FFAR3:free fatty acid receptor 3 [Gene - OMIM - HGNC]
• GAPDHS:glyceraldehyde-3-phosphate dehydrogenase, spermatogenic [Gene - OMIM - HGNC]
• HAMP:hepcidin antimicrobial peptide [Gene - OMIM - HGNC]
• KRTDAP:keratinocyte differentiation associated protein [Gene - OMIM - HGNC]
• LSR:lipolysis stimulated lipoprotein receptor [Gene - OMIM - HGNC]
• MAG:myelin associated glycoprotein [Gene - OMIM - HGNC]
• SBSN:suprabasin [Gene - OMIM - HGNC]
• TMEM147:transmembrane protein 147 [Gene - OMIM - HGNC]
• USF2:upstream transcription factor 2, c-fos interacting [Gene - OMIM - HGNC]
• UPK1A:uroplakin 1A [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

19q13.12

Genomic location:

Chr19: 35658728 - 36173537 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 19q13.12(chr19:35658728-36173537)x3

HGVS:

This HGVS expression did not pass validation