8q11.23 Copy Number Variation
Description
Genomic location GRCh37/hg19
Disorder Information from Orphanet
This CNV is not yet linked to an OrphaCode.
Interactive Pathway Viewer
Gene Information
| HGNC | Gene Name | NCBI | Ensembl | UniProt |
|---|---|---|---|---|
| RB1CC1 | RB1 inducible coiled-coil 1 | 9821 | ENSG00000023287 | Q8TDY2 |