ClinVar

GRCh37/hg19 15q11.2-13.2(chr15:23285775-30386399)

Genes:

• ATP10A:ATPase phospholipid transporting 10A (putative) [Gene - OMIM - HGNC]
• HERC2:HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Gene - OMIM - HGNC]
• MAGEL2:MAGE family member L2 [Gene - OMIM - HGNC]
• NSMCE3:NSE3 homolog, SMC5-SMC6 complex component [Gene - OMIM - HGNC]
• OCA2:OCA2 melanosomal transmembrane protein [Gene - OMIM - HGNC]
• PWAR1:Prader Willi/Angelman region RNA 1 [Gene - OMIM - HGNC]
• PWAR4:Prader Willi/Angelman region RNA 4 [Gene - HGNC]
• PWAR5:Prader Willi/Angelman region RNA 5 [Gene - OMIM - HGNC]
• PWAR6:Prader Willi/Angelman region RNA 6 [Gene - HGNC]
• PWARSN:Prader Willi/Angelman region RNA, SNRPN neighbor [Gene - HGNC]
• PWRN1:Prader-Willi region non-protein coding RNA 1 [Gene - OMIM - HGNC]
• PWRN2:Prader-Willi region non-protein coding RNA 2 [Gene - OMIM - HGNC]
• SNURF:SNRPN upstream open reading frame [Gene - HGNC]
• APBA2:amyloid beta precursor protein binding family A member 2 [Gene - OMIM - HGNC]
• ENTREP2:endosomal transmembrane epsin interactor 2 [Gene - OMIM - HGNC]
• GABRA5:gamma-aminobutyric acid type A receptor subunit alpha5 [Gene - OMIM - HGNC]
• GABRB3:gamma-aminobutyric acid type A receptor subunit beta3 [Gene - OMIM - HGNC]
• GABRG3:gamma-aminobutyric acid type A receptor subunit gamma3 [Gene - OMIM - HGNC]
• GOLGA6L2:golgin A6 family like 2 [Gene - HGNC]
• GOLGA8J:golgin A8 family member J [Gene - HGNC]
• GOLGA8M:golgin A8 family member M [Gene - HGNC]
• IPW:imprinted in Prader-Willi syndrome [Gene - OMIM - HGNC]
• MKRN3:makorin ring finger protein 3 [Gene - OMIM - HGNC]
• NDN:necdin, MAGE family member [Gene - OMIM - HGNC]
• NPAP1:nuclear pore associated protein 1 [Gene - OMIM - HGNC]
• SNRPN:small nuclear ribonucleoprotein polypeptide N [Gene - OMIM - HGNC]
• SNORD115-1:small nucleolar RNA, C/D box 115-1 [Gene - OMIM - HGNC]
• SNORD116-1:small nucleolar RNA, C/D box 116-1 [Gene - OMIM - HGNC]
• TJP1:tight junction protein 1 [Gene - OMIM - HGNC]
• UBE3A:ubiquitin protein ligase E3A [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

15q11.2-13.2

Genomic location:

Chr15: 23285775 - 30386399 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 15q11.2-13.2(chr15:23285775-30386399)