ClinVar

GRCh37/hg19 15q13.1-13.3(chr15:28915863-32446830)x1

Genes:

• CHRFAM7A:CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion [Gene - OMIM - HGNC]
• FAN1:FANCD2 and FANCI associated nuclease 1 [Gene - OMIM - HGNC]
• KLF13:KLF transcription factor 13 [Gene - OMIM - HGNC]
• NSMCE3:NSE3 homolog, SMC5-SMC6 complex component [Gene - OMIM - HGNC]
• OTUD7A:OTU deubiquitinase 7A [Gene - OMIM - HGNC]
• ARHGAP11B:Rho GTPase activating protein 11B [Gene - OMIM - HGNC]
• APBA2:amyloid beta precursor protein binding family A member 2 [Gene - OMIM - HGNC]
• CHRNA7:cholinergic receptor nicotinic alpha 7 subunit [Gene - OMIM - HGNC]
• ENTREP2:endosomal transmembrane epsin interactor 2 [Gene - OMIM - HGNC]
• GOLGA8H:golgin A8 family member H [Gene - HGNC]
• GOLGA8J:golgin A8 family member J [Gene - HGNC]
• GOLGA8M:golgin A8 family member M [Gene - HGNC]
• MIR211:microRNA 211 [Gene - OMIM - HGNC]
• MTMR10:myotubularin related protein 10 [Gene - HGNC]
• TJP1:tight junction protein 1 [Gene - OMIM - HGNC]
• TRPM1:transient receptor potential cation channel subfamily M member 1 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

15q13.1-13.3

Genomic location:

Chr15: 28915863 - 32446830 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 15q13.1-13.3(chr15:28915863-32446830)x1

HGVS:

NC_000015.9:g.(?_28915863)_(32446830_?)del

This HGVS expression did not pass validation