Variants
Found 8 variants in this database.
Variant ID |
Entrez Gene ID |
Gene |
Chromsome |
Start |
End |
Disease |
Method |
13852 |
84898 |
PLXDC2 |
10 |
20397078 |
20397078 |
Asymptomatic
|
HiSeq X Ten
|
13894 |
84898 |
PLXDC2 |
10 |
20301721 |
20301721 |
Asymptomatic
|
HiSeq X Ten
|
13901 |
84898 |
PLXDC2 |
10 |
20193947 |
20193947 |
Asymptomatic
|
HiSeq X Ten
|
14051 |
84898 |
PLXDC2 |
10 |
20619368 |
20619368 |
Asymptomatic
|
HiSeq X Ten
|
14293 |
84898 |
PLXDC2 |
10 |
20820616 |
20820616 |
Asymptomatic
|
HiSeq X Ten
|
14625 |
84898 |
PLXDC2 |
10 |
20188475 |
20188475 |
Asymptomatic
|
HiSeq X Ten
|
14626 |
84898 |
PLXDC2 |
10 |
20457452 |
20457452 |
Asymptomatic
|
HiSeq X Ten
|
14726 |
84898 |
PLXDC2 |
10 |
20389398 |
20389398 |
Cockayne syndrome
|
HiSeq X Ten
|