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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AIFM3, CCDC116
+123 more
Copy number gain
See cases
GPathogenic
GGTLC2, IGL
+37 more
Copy number loss
See cases
GBenign
IGL, PRAME
(W7R)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
BCR, GNAZ
+80 more
Copy number gain
See cases
GPathogenic
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