"GeneDx"[submitter] AND "GPC5"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57644	GRCh38/hg38 13q22.3-32.1(chr13:78349126-94701844)x1	DCT, GPC5 +121 more	Copy number loss	See cases	GPathogenic
Select item 57678	GRCh38/hg38 13q31.2-32.3(chr13:88323009-98888644)x1	ABCC4, CLDN10 +168 more	Copy number loss	See cases	GPathogenic
Select item 58175	GRCh38/hg38 13q31.3(chr13:90973752-93097331)x1	GPC5, GPC5-AS1 +18 more	Copy number loss	See cases	GUncertain significance
Select item 151277	GRCh38/hg38 13q31.3(chr13:91413406-91625217)x1	GPC5	Copy number loss	See cases	GLikely benign
Select item 58176	GRCh38/hg38 13q31.3(chr13:91431897-91628212)x1	GPC5	Copy number loss	See cases	GUncertain significance
Select item 152625	GRCh38/hg38 13q31.3(chr13:91441741-91625217)x1	GPC5	Copy number loss	See cases	GLikely benign
Select item 145224	GRCh38/hg38 13q31.3(chr13:91521052-91597567)x1	GPC5	Copy number loss	See cases	GBenign/Likely benign
Select item 253830	GRCh37/hg19 13q31.3(chr13:91209639-94704856)x3	GPC5, GPC6 +7 more	Copy number gain	See cases	GUncertain significance
Select item 253491	GRCh37/hg19 13q31.2-34(chr13:89796110-115083342)x1	ABCC4, ABHD13 +94 more	Copy number loss	See cases	GPathogenic
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic