Variants
Found 7 variants in this database.
Variant ID |
Entrez Gene ID |
Gene |
Chromsome |
Start |
End |
Disease |
Method |
20914 |
374900 |
ZNF568 |
19 |
37547877 |
37547877 |
Asymptomatic
|
HiSeq X Ten
|
20928 |
374900 |
ZNF568 |
19 |
37425332 |
37425332 |
Asymptomatic
|
HiSeq X Ten
|
20977 |
374900 |
ZNF568 |
19 |
37504664 |
37504664 |
Asymptomatic
|
HiSeq X Ten
|
20987 |
374900 |
ZNF568 |
19 |
37497125 |
37497125 |
Asymptomatic
|
HiSeq X Ten
|
21050 |
374900 |
ZNF568 |
19 |
37442504 |
37442504 |
Cockayne syndrome
|
HiSeq X Ten
|
21062 |
374900 |
ZNF568 |
19 |
37447723 |
37447723 |
Cockayne syndrome
|
HiSeq X Ten
|
28460 |
374900 |
ZNF568 |
19 |
37544798 |
37544798 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|