ClinVar

GRCh37/hg19 15q24.1-24.2(chr15:72943184-76085232)

Genes:

• ADPGK:ADP dependent glucokinase [Gene - OMIM - HGNC]
• ARID3B:AT-rich interaction domain 3B [Gene - OMIM - HGNC]
• BBS4:Bardet-Biedl syndrome 4 [Gene - OMIM - HGNC]
• CSK:C-terminal Src kinase [Gene - OMIM - HGNC]
• CD276:CD276 molecule [Gene - OMIM - HGNC]
• CLK3:CDC like kinase 3 [Gene - OMIM - HGNC]
• COMMD4:COMM domain containing 4 [Gene - OMIM - HGNC]
• IMP3:IMP U3 small nucleolar ribonucleoprotein 3 [Gene - OMIM - HGNC]
• PML:PML nuclear body scaffold [Gene - OMIM - HGNC]
• REC114:REC114 meiotic recombination protein [Gene - OMIM - HGNC]
• SIN3A:SIN3 transcription regulator family member A [Gene - OMIM - HGNC]
• TBC1D21:TBC1 domain family member 21 [Gene - OMIM - HGNC]
• CSPG4:chondroitin sulfate proteoglycan 4 [Gene - OMIM - HGNC]
• C15orf39:chromosome 15 open reading frame 39 [Gene - HGNC]
• CIMAP1C:ciliary microtubule associated protein 1C [Gene - HGNC]
• CCDC33:coiled-coil domain containing 33 [Gene - OMIM - HGNC]
• CPLX3:complexin 3 [Gene - OMIM - HGNC]
• CYP1A1:cytochrome P450 family 1 subfamily A member 1 [Gene - OMIM - HGNC]
• CYP1A2:cytochrome P450 family 1 subfamily A member 2 [Gene - OMIM - HGNC]
• CYP11A1:cytochrome P450 family 11 subfamily A member 1 [Gene - OMIM - HGNC]
• COX5A:cytochrome c oxidase subunit 5A [Gene - OMIM - HGNC]
• EDC3:enhancer of mRNA decapping 3 [Gene - OMIM - HGNC]
• FAM219B:family with sequence similarity 219 member B [Gene - HGNC]
• GOLGA6A:golgin A6 family member A [Gene - OMIM - HGNC]
• GOLGA6B:golgin A6 family member B [Gene - HGNC]
• GOLGA6C:golgin A6 family member C [Gene - HGNC]
• GOLGA6D:golgin A6 family member D [Gene - HGNC]
• HCN4:hyperpolarization activated cyclic nucleotide gated potassium channel 4 [Gene - OMIM - HGNC]
• ISLR2:immunoglobulin superfamily containing leucine rich repeat 2 [Gene - OMIM - HGNC]
• ISLR:immunoglobulin superfamily containing leucine rich repeat [Gene - OMIM - HGNC]
• INSYN1:inhibitory synaptic factor 1 [Gene - OMIM - HGNC]
• LMAN1L:lectin, mannose binding 1 like [Gene - OMIM - HGNC]
• LOXL1:lysyl oxidase like 1 [Gene - OMIM - HGNC]
• MPI:mannose phosphate isomerase [Gene - OMIM - HGNC]
• MAN2C1:mannosidase alpha class 2C member 1 [Gene - OMIM - HGNC]
• NEIL1:nei like DNA glycosylase 1 [Gene - OMIM - HGNC]
• NEO1:neogenin 1 [Gene - OMIM - HGNC]
• NPTN:neuroplastin [Gene - OMIM - HGNC]
• PPCDC:phosphopantothenoylcysteine decarboxylase [Gene - OMIM - HGNC]
• PTPN9:protein tyrosine phosphatase non-receptor type 9 [Gene - OMIM - HGNC]
• RPP25:ribonuclease P and MRP subunit p25 [Gene - OMIM - HGNC]
• SCAMP2:secretory carrier membrane protein 2 [Gene - OMIM - HGNC]
• SCAMP5:secretory carrier membrane protein 5 [Gene - OMIM - HGNC]
• SEMA7A:semaphorin 7A (JohnMiltonHagen blood group) [Gene - OMIM - HGNC]
• STRA6:signaling receptor and transporter of retinol STRA6 [Gene - OMIM - HGNC]
• SNUPN:snurportin 1 [Gene - OMIM - HGNC]
• SNX33:sorting nexin 33 [Gene - OMIM - HGNC]
• STOML1:stomatin like 1 [Gene - OMIM - HGNC]
• UBL7:ubiquitin like 7 [Gene - OMIM - HGNC]
• ULK3:unc-51 like kinase 3 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

15q24.1-24.2

Genomic location:

Chr15: 72943184 - 76085232 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 15q24.1-24.2(chr15:72943184-76085232)