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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TUBGCP5
(F727C +2 more)
Single nucleotide variant
(missense variant +1 more)
Microcephaly
GUncertain significance
CYFIP1, NIPA1
+2 more
Copy number loss
Abnormal facial shape
+9 more
GPathogenic
CYFIP1, GOLGA6L1
+3 more
Copy number loss
Global developmental delay
GPathogenic
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