ID: 107985085 | uncharacterized LOC107985085 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43674990..43690763, complement) | | |
ID: 107985077 | uncharacterized LOC107985077 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43849750..43854590, complement) | | |
ID: 107984979 | uncharacterized LOC107984979 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43833705..43846617) | | |
ID: 106660605 | MIR2117 host gene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43444707..43451197) | | |
ID: 106481926 | RNA, U6 small nuclear 971, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43473585..43473690) | | |
ID: 106481306 | RNA, U6 small nuclear 406, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43445507..43445613) | | |
ID: 106480067 | RNA, U6 small nuclear 1137, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43395993..43396091, complement) | | |
ID: 106479773 | RNA, U6 small nuclear 470, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43412427..43412530) | | |
ID: 105371786 | long intergenic non-protein coding RNA 2594 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43664864..43706758) | | |
ID: 105371785 | uncharacterized LOC105371785 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43368636..43373809) | | |
ID: 101929767 | uncharacterized LOC101929767 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43148366..43170403, complement) | | |
ID: 100885865 | high mobility group nucleosome binding domain 1 pseudogene 29 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43144845..43145323) | | |
ID: 100874261 | coiled-coil domain containing 200 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43221417..43231269, complement) | LINC00854, TMEM106A-AS1 | |
ID: 100313779 | microRNA 2117 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43444806..43444885) | | |
ID: 100130581 | long intergenic non-protein coding RNA 910 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43369845..43388898, complement) | | |
ID: 100128016 | Wolf-Hirschhorn syndrome candidate 1-like 2, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43718314..43720436, complement) | HsT36289, NSD4P, WHSC1L1P | |
ID: 394269 | BRCA1 pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43168070..43169954, complement) | LBRCA1, PsiBRCA1, pseudo-BRCA1 | |
ID: 284067 | CFAP97 domain containing 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43780435..43787620) | C17orf105 | 619866 |
ID: 284064 | ribosomal protein L29 pseudogene 31 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43476154..43476765) | PERMIT, RPL29_11_1549, p17 | |
ID: 146894 | CD300 molecule like family member g [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43847176..43863639) | CLM-9, CLM9, NEPMUCIN, TREM-4, TREM4 | 610520 |