Found 9 variants in this database.
Variant ID |
Entrez Gene ID |
Gene |
Chromsome |
Start |
End |
Disease |
Method |
22014 |
170062 |
FAM47B |
X |
35782917 |
35782917 |
Asymptomatic
|
HiSeq X Ten
|
22068 |
170062 |
FAM47B |
X |
35129357 |
35129357 |
Asymptomatic
|
HiSeq X Ten
|
22184 |
170062 |
FAM47B |
X |
35355920 |
35355920 |
Asymptomatic
|
HiSeq X Ten
|
24181 |
170062 |
FAM47B |
X |
35416330 |
35416330 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|
28758 |
170062 |
FAM47B |
X |
35664239 |
35664239 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|
28759 |
170062 |
FAM47B |
X |
35770880 |
35770880 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|
28820 |
170062 |
FAM47B |
X |
35770880 |
35770880 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|
28832 |
170062 |
FAM47B |
X |
35770880 |
35770880 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|
28961 |
170062 |
FAM47B |
X |
35623649 |
35623649 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|