"GeneDx"[submitter] AND "CDH12"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59604	GRCh38/hg38 5p15.2-14.3(chr5:13609772-21930280)x1	ANKH, BASP1 +142 more	Copy number loss	See cases	GPathogenic
Select item 60257	GRCh38/hg38 5p14.3(chr5:21852725-21964074)x1	CDH12, SNORA105A	Copy number loss	See cases	GUncertain significance
Select item 151663	GRCh38/hg38 5p14.3-14.2(chr5:22002509-23432919)x3	CDH12, LOC123493278 +4 more	Copy number gain	See cases	GLikely benign
Select item 253597	GRCh37/hg19 5p15.2-12(chr5:13461664-46098927)x3	RXFP3, GDNF +89 more	Copy number gain	See cases	GPathogenic
Select item 253537	GRCh37/hg19 5p15.33-13.2(chr5:22149-34041255)x3	AHRR, ADAMTS12 +82 more	Copy number gain	See cases	GPathogenic

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