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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59977	GRCh38/hg38 20q12(chr20:41822419-42468515)x1	LOC129391177, LOC129391178 +1 more	Copy number loss	See cases	GUncertain significance
Select item 1285993	NM_007050.6(PTPRT):c.*1640G>A	PTPRT	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 145099	GRCh38/hg38 20q12(chr20:42438777-42478707)x3	PTPRT	Copy number gain	See cases	GBenign
Select item 152801	GRCh38/hg38 20q12(chr20:42478707-42551910)x1	PTPRT	Copy number loss	See cases	GUncertain significance
Select item 59978	GRCh38/hg38 20q12(chr20:42560011-42713556)x1	LOC101927159, PTPRT	Copy number loss	See cases	GUncertain significance
Select item 145297	GRCh38/hg38 20q12(chr20:42596264-42683848)x1	PTPRT	Copy number loss	See cases	GBenign
Select item 1241839	NM_007050.6(PTPRT):c.1153+7dup	PTPRT	Duplication (intron variant)	not provided	GBenign
Select item 1226281	NM_007050.6(PTPRT):c.1059T>C (p.Asp353=)	PTPRT	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar