ClinVar

GRCh37/hg19 15q26.1(chr15:91229877-93677014)x1

Genes:

• BLM:BLM RecQ like helicase [Gene - OMIM - HGNC]
• FES:FES proto-oncogene, tyrosine kinase [Gene - OMIM - HGNC]
• HDDC3:HD domain containing 3 [Gene - HGNC]
• RCCD1:RCC1 domain containing 1 [Gene - OMIM - HGNC]
• ST8SIA2:ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 [Gene - OMIM - HGNC]
• VPS33B:VPS33B late endosome and lysosome associated [Gene - OMIM - HGNC]
• CHD2:chromodomain helicase DNA binding protein 2 [Gene - OMIM - HGNC]
• C15orf32:chromosome 15 putative open reading frame 32 [Gene - HGNC]
• FAM174B:family with sequence similarity 174 member B [Gene - HGNC]
• FURIN:furin, paired basic amino acid cleaving enzyme [Gene - OMIM - HGNC]
• MAN2A2:mannosidase alpha class 2A member 2 [Gene - OMIM - HGNC]
• PRC1:protein regulator of cytokinesis 1 [Gene - OMIM - HGNC]
• RGMA:repulsive guidance molecule BMP co-receptor a [Gene - OMIM - HGNC]
• SLCO3A1:solute carrier organic anion transporter family member 3A1 [Gene - OMIM - HGNC]
• SV2B:synaptic vesicle glycoprotein 2B [Gene - OMIM - HGNC]
• UNC45A:unc-45 myosin chaperone A [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

15q26.1

Genomic location:

Chr15: 91229877 - 93677014 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 15q26.1(chr15:91229877-93677014)x1

HGVS:

NC_000015.9:g.(?_91229877)_(93677014_?)del

This HGVS expression did not pass validation