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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC123453201, LOC123453202
+1450 more
Copy number gain
See cases
GPathogenic
LOC132088897, LOC132088898
+1201 more
Copy number gain
See cases
GPathogenic
MIR944, MUC20
+557 more
Copy number loss
See cases
GPathogenic
RUBCN, SENP5
+264 more
Copy number gain
See cases
GPathogenic
DYNLT2B, LINC00885
+41 more
Copy number gain
See cases
GUncertain significance
DYNLT2B
Single nucleotide variant
(intron variant)
not provided
GBenign
DYNLT2B
Single nucleotide variant
(intron variant)
not provided
GBenign
DYNLT2B
Single nucleotide variant
(intron variant)
not provided
GBenign
DYNLT2B
Single nucleotide variant
(intron variant)
not provided
GBenign
DYNLT2B, TM4SF19-DYNLT2B
Duplication
(intron variant)
not provided
GBenign
DYNLT2B, LOC129938284
+1 more
Single nucleotide variant
(intron variant)
not provided
GBenign
DYNLT2B, LOC129938284
+1 more
Single nucleotide variant
(intron variant)
not provided
GBenign
DYNLT2B, TM4SF19-DYNLT2B
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
NRROS, SENP5
+19 more
Copy number loss
See cases
GPathogenic
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