| ID: 6103 | retinitis pigmentosa GTPase regulator [Homo sapiens (human)] | Chromosome X, NC_000023.11 (38269163..38327509, complement) | COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15 | 312610 |
| ID: 257415 | family with sequence similarity 133 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92560758..92590390, complement) | | |
| ID: 51142 | coiled-coil-helix-coiled-coil-helix domain containing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (56101573..56106476, complement) | C7orf17, MIX17B, MNRR1, NS2TP, PARK22 | 616244 |