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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130001226, LOC130001227
+1407 more
Copy number gain
See cases
GPathogenic
ADGRB1, ARC
+172 more
Copy number loss
See cases
GPathogenic
TOP1MT
(V158I +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
LOC113788265, LOC130001324
+13 more
Copy number gain
See cases
GUncertain significance
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