"ISCA site 4"[submitter] AND "PRKN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57020	GRCh38/hg38 6q24.1-27(chr6:141132990-169339571)x3	LOC129389719, LOC129389720 +866 more	Copy number gain	See cases	GPathogenic
Select item 144539	GRCh38/hg38 6q25.3-27(chr6:160484810-170612011)x1	AFDN, AFDN-DT +298 more	Copy number loss	See cases	GPathogenic
Select item 146832	GRCh38/hg38 6q26(chr6:162163288-162819968)x3	LOC126859871, PACRG +1 more	Copy number gain	See cases	GUncertain significance
Select item 154967	GRCh38/hg38 6q26(chr6:162232971-162629368)x3	PRKN	Copy number gain	See cases	GLikely benign
Select item 150700	GRCh38/hg38 6q26(chr6:162232971-162629368)x1	PRKN	Copy number loss	See cases	GUncertain significance
Select item 145398	GRCh38/hg38 6q26(chr6:162232971-162708613)x3	PRKN	Copy number gain	See cases	GUncertain significance
Select item 146769	GRCh38/hg38 6q26(chr6:162327214-162629368)x3	PRKN	Copy number gain	See cases	GUncertain significance

ClinVar