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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NIPBL
(G519*)
Single nucleotide variant
(nonsense)
Cornelia de Lange syndrome 1
GPathogenic
NIPBL
(N764fs)
Deletion
(frameshift variant)
Cornelia de Lange syndrome 1
GPathogenic
NIPBL
(R827fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
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