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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130056392, LOC130056393
+1073 more
Copy number gain
See cases
GPathogenic
ASB2, ATXN3
+201 more
Copy number loss
See cases
GPathogenic
CCDC88C, LOC130056326
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
CCDC88C, LOC130056326
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
CCDC88C, LOC130056326
Single nucleotide variant
not provided
GBenign
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