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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC613266, MACROD2
+950 more
Copy number gain
See cases
GPathogenic
ESF1, FLRT3
+26 more
Copy number gain
See cases
GUncertain significance
ESF1, LOC113939992
+5 more
Copy number gain
See cases
GUncertain significance
LOC130065434, NDUFAF5
Single nucleotide variant
(intron variant)
not provided
GBenign
LOC130065434, NDUFAF5
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
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