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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC88A, CFAP36
+8 more
Copy number gain
not provided
GUncertain significance
EML6, RTN4
+1 more
Copy number gain
not provided
GUncertain significance
ABCG5, ABCG8
+100 more
Copy number gain
not provided
GPathogenic
GPR75, TSPYL6
+7 more
Copy number gain
not provided
GLikely benign
EML6
Copy number loss
not provided
GUncertain significance
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