"GeneDx"[submitter] AND "PDCD6-AHRR"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152421	GRCh38/hg38 5p15.33(chr5:22149-356107)x1	AHRR, CCDC127 +24 more	Copy number loss	See cases	GLikely benign
Select item 151630	GRCh38/hg38 5p15.33(chr5:22149-658446)x1	LOC132089252, LOC132089253 +75 more	Copy number loss	See cases	GLikely benign
Select item 146067	GRCh38/hg38 5p15.33(chr5:22149-1278576)x3	LOC132089294, LOC132089295 +113 more	Copy number gain	See cases	GUncertain significance
Select item 59557	GRCh38/hg38 5p15.33(chr5:22149-3556942)x1	AHRR, BRD9 +194 more	Copy number loss	See cases	GPathogenic
Select item 59578	GRCh38/hg38 5p15.33(chr5:37694-2913205)x1	LOC132090723, LOC132090724 +182 more	Copy number loss	See cases	GPathogenic
Select item 59577	GRCh38/hg38 5p15.33(chr5:37694-2746908)x1	AHRR, BRD9 +180 more	Copy number loss	See cases	GPathogenic
Select item 59601	GRCh38/hg38 5p15.33-15.32(chr5:54839-5603401)x1	ADAMTS16, ADAMTS16-DT +226 more	Copy number loss	See cases	GPathogenic
Select item 145235	GRCh38/hg38 5p15.33(chr5:234045-292564)x3	LOC129993531, LOC129993532 +4 more	Copy number gain	See cases	GBenign
Select item 151631	GRCh38/hg38 5p15.33(chr5:314795-496067)x1	AHRR, EXOC3 +49 more	Copy number loss	See cases	GBenign
Select item 57919	GRCh38/hg38 5p15.33(chr5:316478-937457)x3	AHRR, BRD9 +84 more	Copy number gain	See cases	GUncertain significance
Select item 145222	GRCh38/hg38 5p15.33(chr5:346162-404606)x3	AHRR, LOC126807281 +14 more	Copy number gain	See cases	GBenign