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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130055392, LOC130055393
+780 more
Copy number gain
See cases
GPathogenic
ABHD4, ACIN1
+814 more
Copy number gain
See cases
GPathogenic
OR10G2, OR10G3
+859 more
Copy number gain
See cases
GPathogenic
LOC125048431, LOC125048432
+3280 more
Copy number gain
See cases
GPathogenic
FSCB, FUT8
+3275 more
Copy number gain
See cases
GPathogenic
LOC112214170, LOC112214171
+840 more
Copy number loss
See cases
GPathogenic
MIR4503, MIR624
+399 more
Copy number loss
See cases
GPathogenic
AKAP6, AP4S1
+73 more
Copy number loss
See cases
GPathogenic
AKAP6, AP4S1
+179 more
Copy number loss
See cases
GPathogenic
INSM2, KLHL28
+237 more
Copy number gain
See cases
GPathogenic
LOC126861917, LOC126861918
+225 more
Copy number loss
See cases
GPathogenic
ARHGAP5-AS1, DTD2
+35 more
Deletion
Mitochondrial complex I deficiency
GUncertain significance
DTD2, GPR33
+9 more
Copy number loss
See cases
GUncertain significance
DTD2, GPR33
+10 more
Copy number loss
See cases
GUncertain significance
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