"GeneDx"[submitter] AND "PTK2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144949	GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3	LOC130001226, LOC130001227 +1407 more	Copy number gain	See cases	GPathogenic
Select item 1226102	NM_001352702.2(PTK2):c.*705T>A	PTK2	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1266242	NM_001352702.2(PTK2):c.1177+9092T>G	PTK2	Single nucleotide variant (intron variant)	not provided	GBenign

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