ClinVar

GRCh37/hg19 4q31.3-32.1(chr4:154907679-159012980)x1

Genes:

• RBM46:RNA binding motif protein 46 [Gene - HGNC]
• ASIC5:acid sensing ion channel subunit family member 5 [Gene - OMIM - HGNC]
• CTSO:cathepsin O [Gene - OMIM - HGNC]
• DCHS2:dachsous cadherin-related 2 [Gene - OMIM - HGNC]
• FGA:fibrinogen alpha chain [Gene - OMIM - HGNC]
• FGB:fibrinogen beta chain [Gene - OMIM - HGNC]
• FGG:fibrinogen gamma chain [Gene - OMIM - HGNC]
• GRIA2:glutamate ionotropic receptor AMPA type subunit 2 [Gene - OMIM - HGNC]
• GLRB:glycine receptor beta [Gene - OMIM - HGNC]
• GUCY1A1:guanylate cyclase 1 soluble subunit alpha 1 [Gene - OMIM - HGNC]
• GUCY1B1:guanylate cyclase 1 soluble subunit beta 1 [Gene - OMIM - HGNC]
• LRAT:lecithin retinol acyltransferase [Gene - OMIM - HGNC]
• MAP9:microtubule associated protein 9 [Gene - OMIM - HGNC]
• NPY2R:neuropeptide Y receptor Y2 [Gene - OMIM - HGNC]
• PDGFC:platelet derived growth factor C [Gene - OMIM - HGNC]
• PLRG1:pleiotropic regulator 1 [Gene - OMIM - HGNC]
• TDO2:tryptophan 2,3-dioxygenase [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

4q31.3-32.1

Genomic location:

Chr4: 154907679 - 159012980 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 4q31.3-32.1(chr4:154907679-159012980)x1

HGVS:

NC_000004.11:g.(?_154907679)_(159012980_?)del

This HGVS expression did not pass validation