"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PARG"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2640464	NM_003631.2(PARG):c.1455+115464A>G	PARG	Single nucleotide variant	not provided	GLikely benign
Select item 1879150	GRCh37/hg19 10q11.22-11.23(chr10:46584432-51974628)x3	ANXA8L1, AGAP9 +35 more	Copy number gain	not provided	GUncertain significance
Select item 624468	GRCh37/hg19 10q11.22-21.1(chr10:49390457-60061643)x1	MSMB, MTRNR2L5 +33 more	Copy number loss	not provided	GLikely pathogenic

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