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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC123775388, LOC123775389
+1449 more
Copy number gain
See cases
GPathogenic
AKAP7, ARG1
+400 more
Deletion
Interstitial 6q microdeletion syndrome
GPathogenic
AKAP7, ARG1
+127 more
Copy number loss
See cases
GLikely pathogenic
CCN2, CCN2-AS1
+14 more
Deletion
Arterial calcification, generalized, of infancy, 1
GPathogenic
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