ID: 123464521 | inward rectifying K+ channel negative regulator Kir2.2v [Homo sapiens (human)] | | KCNJN1, Kir2.2v, Kir2.5 | |
ID: 111188157 | LYNX1-SLURP2 readthrough [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142764338..142777872, complement) | | |
ID: 107986810 | Williams-Beuren syndrome chromosome region 23 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74532592..74533213) | | |
ID: 107985820 | CNTNAP5 divergent transcript [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (124011934..124025174, complement) | | |
ID: 105378803 | leucine rich repeat containing 53 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (74469376..74537079, complement) | | |
ID: 105378085 | uncharacterized LOC105378085 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (159586953..159595632, complement) | | |
ID: 105376204 | uncharacterized LOC105376204 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (106852961..106860520, complement) | | |
ID: 105372280 | G protein subunit gamma 14 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12687998..12688422) | HG3K | |
ID: 102724928 | cyclin Y like 3 (pseudogene) [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (35030349..35060328) | CCNYL1B | |
ID: 102723968 | uncharacterized LOC102723968 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (63828840..63844125, complement) | | |
ID: 102723566 | uncharacterized LOC102723566 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127816066..127822520) | | |
ID: 101929926 | testis expressed 51 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (126898890..126902097) | | |
ID: 101929637 | NTM antisense RNA 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (131662129..131663556, complement) | C11orf39 | |
ID: 101928764 | coiled-coil domain-containing protein 144B [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (21283487..21298091, complement) | | |
ID: 101928697 | Putative uncharacterized protein LOC645739 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (19182033..19187465) | | |
ID: 101928343 | uncharacterized LOC101928343 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (74599840..74625996) | | |
ID: 101927581 | coiled-coil domain containing 182 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57744495..57745299, complement) | | |
ID: 101752399 | STAG3L5P-PVRIG2P-PILRB readthrough [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100336065..100367831) | FDFACT, LOC101735302-LOC101752334-PILRB, PILRB | |
ID: 101060200 | zinc finger protein 891 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (133104779..133130274, complement) | | |
ID: 100996792 | dual specificity mitogen-activated protein kinase kinase 3 pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (21772755..21783465, complement) | | |