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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129929262, LOC129929263
+458 more
Copy number loss
See cases
GPathogenic
LINC01786, LINC02593
+338 more
Copy number gain
See cases
GPathogenic
ACAP3, AGRN
+246 more
Copy number gain
See cases
GPathogenic
ACAP3, ACTRT2
+273 more
Copy number loss
See cases
GPathogenic
LOC121967044, TMEM240
Single nucleotide variant
(intron variant)
not provided
GBenign
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