"GeneDx"[submitter] AND "CPLANE1-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58092	GRCh38/hg38 5p13.2-12(chr5:35700480-45260029)x3	LOC126807367, LOC126807368 +254 more	Copy number gain	See cases	GPathogenic
Select item 58093	GRCh38/hg38 5p13.2-q11.1(chr5:36374107-51103841)x3	ANXA2R, ANXA2R-AS1 +245 more	Copy number gain	See cases	GPathogenic
Select item 57962	GRCh38/hg38 5p13.2(chr5:36886533-37331810)x3	CPLANE1, CPLANE1-AS1 +9 more	Copy number gain	See cases	GUncertain significance
Select item 57963	GRCh38/hg38 5p13.2(chr5:36906275-37606265)x3	CPLANE1, CPLANE1-AS1 +19 more	Copy number gain	See cases	GUncertain significance
Select item 151661	GRCh38/hg38 5p13.2(chr5:37150088-37364068)x3	CPLANE1, CPLANE1-AS1 +7 more	Copy number gain	See cases	GLikely benign
Select item 57964	GRCh38/hg38 5p13.2(chr5:37157004-37571897)x3	CPLANE1, CPLANE1-AS1 +16 more	Copy number gain	See cases	GUncertain significance
Select item 152878	GRCh38/hg38 5p13.2(chr5:37239106-37487479)x3	CPLANE1, CPLANE1-AS1 +10 more	Copy number gain	See cases	GUncertain significance
Select item 152428	GRCh38/hg38 5p13.2(chr5:37239106-37298497)x4	CPLANE1, CPLANE1-AS1 +4 more	Copy number gain	See cases	GUncertain significance
Select item 152427	GRCh38/hg38 5p13.2(chr5:37239106-37298497)x3	CPLANE1, CPLANE1-AS1 +4 more	Copy number gain	See cases	GLikely benign
Select item 510602	NM_001384732.1(CPLANE1):c.-48+10C>A	CPLANE1, CPLANE1-AS1 +1 more	Single nucleotide variant (intron variant)	not specified	GLikely benign