| Entrez Gene ID | 83641 |
|---|---|
| Official Gene Symbol | FAM107B (GeneCards) |
| Full name | family with sequence similarity 107 member B |
| Location | 10p13 |
| Other ids | Vega : OTTHUMG00000017709 HGNC : HGNC:23726 Ensembl : ENSG00000065809 |
| Other names | HITS, C10orf45 |
| Summary | None |
Found 7 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 13905 | 83641 | FAM107B | 10 | 14840468 | 14840468 | Asymptomatic | HiSeq X Ten |
| 14001 | 83641 | FAM107B | 10 | 14849067 | 14849067 | Asymptomatic | HiSeq X Ten |
| 14013 | 83641 | FAM107B | 10 | 14743967 | 14743967 | Asymptomatic | HiSeq X Ten |
| 14755 | 83641 | FAM107B | 10 | 14735346 | 14735346 | Cockayne syndrome | HiSeq X Ten |
| 14945 | 83641 | FAM107B | 10 | 14701359 | 14701359 | Xeroderma Pigmentosum | HiSeq X Ten |
| 14946 | 83641 | FAM107B | 10 | 14757690 | 14757690 | Xeroderma Pigmentosum | HiSeq X Ten |
| 27071 | 83641 | FAM107B | 10 | 14714044 | 14714044 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |