ClinVar

GRCh37/hg19 3p26.3-25.3(chr3:61891-8777555)x1

Genes:

• ARL8B:ADP ribosylation factor like GTPase 8B [Gene - OMIM - HGNC]
• EDEM1:ER degradation enhancing alpha-mannosidase like protein 1 [Gene - OMIM - HGNC]
• LMCD1:LIM and cysteine rich domains 1 [Gene - OMIM - HGNC]
• SETMAR:SET domain and mariner transposase fusion gene [Gene - OMIM - HGNC]
• BHLHE40:basic helix-loop-helix family member e40 [Gene - OMIM - HGNC]
• CAV3:caveolin 3 [Gene - OMIM - HGNC]
• CHL1:cell adhesion molecule L1 like [Gene - OMIM - HGNC]
• CRBN:cereblon [Gene - OMIM - HGNC]
• CNTN4:contactin 4 [Gene - OMIM - HGNC]
• CNTN6:contactin 6 [Gene - OMIM - HGNC]
• EGOT:eosinophil granule ontogeny transcript [Gene - OMIM - HGNC]
• GRM7:glutamate metabotropic receptor 7 [Gene - OMIM - HGNC]
• ITPR1:inositol 1,4,5-trisphosphate receptor type 1 [Gene - OMIM - HGNC]
• IL5RA:interleukin 5 receptor subunit alpha [Gene - OMIM - HGNC]
• LRRN1:leucine rich repeat neuronal 1 [Gene - OMIM - HGNC]
• LINC00312:long intergenic non-protein coding RNA 312 [Gene - OMIM - HGNC]
• SSUH2:ssu-2 homolog [Gene - OMIM - HGNC]
• SUMF1:sulfatase modifying factor 1 [Gene - OMIM - HGNC]
• TRNT1:tRNA nucleotidyl transferase 1 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

3p26.3-25.3

Genomic location:

Chr3: 61891 - 8777555 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 3p26.3-25.3(chr3:61891-8777555)x1

HGVS:

NC_000003.11:g.(?_61891)_(8777555_?)del

This HGVS expression did not pass validation

Links:

dbVar: nssv13651647; dbVar: nsv2776623

Observations:

1