ID: 107126285 | septin 14 pseudogene 20 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (64290385..64303354) | C20orf69, LINC00266-1, NCRNA00266, NCRNA00266-1, RBRP, SEPT14P20, bA476I15.3 | |
ID: 100874392 | ankyrin repeat domain 20 family member A12, pseudogene [Homo sapiens (human)] | NT_113793.3 (161987..178171, complement) | | |
ID: 100861402 | CERS6 antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (168771951..168786429, complement) | | |
ID: 100820829 | myocardial zonula adherens protein [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (57591904..57685364) | CMD2K, GCOM1, Gup, MYOZAP | 614071 |
ID: 100775104 | KLHL7 divergent transcript [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (23101228..23105703, complement) | KLHL7-AS1, PLATAK | |
ID: 100750247 | HIF1A antisense RNA 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (61747039..61749089, complement) | 3'aHIF-1A, aHIF | 614529 |
ID: 100653515 | CEP295 N-terminal like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78890579..78903201, complement) | DDC8, KIAA1731NL | |
ID: 100631383 | FAM47E-STBD1 readthrough [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (76251721..76311130) | FAM47E | |
ID: 100630918 | promoter of MAT2A antisense radiation-induced circulating long non-coding RNA [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (85537467..85538886, complement) | PARTICLE | 616350 |
ID: 100616668 | TPTE2 pseudogene 5 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40796985..40921750, complement) | | |
ID: 100616376 | microRNA 4492 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (118910708..118910787) | mir-4492 | |
ID: 100616364 | microRNA 4785 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (160407810..160407882, complement) | mir-4785 | |
ID: 100616318 | microRNA 4664 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143733083..143733153, complement) | | |
ID: 100616122 | microRNA 4523 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (29390662..29390730) | | |
ID: 100534611 | TM4SF19-DYNLT2B readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196316085..196338420, complement) | TM4SF19-TCTEX1D2 | |
ID: 100534593 | STX16-NPEPL1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58651253..58715844) | | |
ID: 100533955 | SENP3-EIF4A1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7561992..7579006) | | |
ID: 100533952 | RBAK-RBAKDN readthrough [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (5045860..5073221) | RBAK, RBAK-LOC389458, ZNF769, hRBaK | |
ID: 100533496 | TVP23C-CDRT4 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15436015..15563483, complement) | FAM18B2, FAM18B2-CDRT4, TVP23C | |
ID: 100533467 | BIVM-ERCC5 readthrough [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102807146..102875995) | ERCC5-202 | |