ClinVar

GRCh37/hg19 2p23.3(chr2:24315204-26384655)x3

Genes:

• ASXL2:ASXL transcriptional regulator 2 [Gene - OMIM - HGNC]
• DNMT3A:DNA methyltransferase 3 alpha [Gene - OMIM - HGNC]
• DNAJC27:DnaJ heat shock protein family (Hsp40) member C27 [Gene - OMIM - HGNC]
• EFR3B:EFR3 homolog B [Gene - OMIM - HGNC]
• RAB10:RAB10, member RAS oncogene family [Gene - OMIM - HGNC]
• ADCY3:adenylate cyclase 3 [Gene - OMIM - HGNC]
• CENPO:centromere protein O [Gene - OMIM - HGNC]
• DTNB:dystrobrevin beta [Gene - OMIM - HGNC]
• FAM228A:family with sequence similarity 228 member A [Gene - HGNC]
• FAM228B:family with sequence similarity 228 member B [Gene - HGNC]
• ITSN2:intersectin 2 [Gene - OMIM - HGNC]
• KIF3C:kinesin family member 3C [Gene - OMIM - HGNC]
• NCOA1:nuclear receptor coactivator 1 [Gene - OMIM - HGNC]
• PTRHD1:peptidyl-tRNA hydrolase domain containing 1 [Gene - OMIM - HGNC]
• PFN4:profilin family member 4 [Gene - HGNC]
• POMC:proopiomelanocortin [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

2p23.3

Genomic location:

Chr2: 24315204 - 26384655 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 2p23.3(chr2:24315204-26384655)x3

HGVS:

This HGVS expression did not pass validation