| ID: 399687 | myosin XVIIIA [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (29071122..29180398, complement) | MAJN, MYSPDZ, SP-R210, SPR210, TIAF1 | 609517, 610067 |
| ID: 64112 | modulator of apoptosis 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (93182199..93184897, complement) | MAP-1, PNMA4 | 609485 |
| ID: 80213 | TM2 domain containing 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (101632977..101652381, complement) | BLP2 | 610014 |
| ID: 83693 | hydroxysteroid dehydrogenase like 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (84122141..84145177, complement) | SDR12C3 | 619067 |
| ID: 23293 | SMG6 nonsense mediated mRNA decay factor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (2059839..2303785, complement) | C17orf31, EST1A, SMG-6, hEST1A, hSMG5/7a | 610963 |
| ID: 26267 | F-box protein 10 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (37510892..37576380, complement) | FBX10, PRMT11 | 609092 |
| ID: 9990 | solute carrier family 12 member 6 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (34229784..34338057, complement) | ACCPN, CMT2II, KCC3, KCC3A, KCC3B | 604878 |
| ID: 23078 | von Willebrand factor A domain containing 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41566835..41961109, complement) | KIAA0564, P7BP2, RP97 | 617509 |
| ID: 152006 | ring finger protein 38 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (36336400..36487669, complement) | | 612488 |