"GeneDx"[submitter] AND "HDAC9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58518	GRCh38/hg38 7p21.3-21.1(chr7:9975653-19356878)x1	AGMO, AGR2 +130 more	Copy number loss	See cases	GPathogenic
Select item 59679	GRCh38/hg38 7p21.2-15.2(chr7:16234212-26167278)x3	ABCB5, AGR2 +287 more	Copy number gain	See cases	GPathogenic
Select item 152081	GRCh38/hg38 7p21.1(chr7:17847049-18321295)x3	HDAC9, LOC111591502 +8 more	Copy number gain	See cases	GBenign
Select item 58533	GRCh38/hg38 7p21.1(chr7:17930595-18209019)x1	HDAC9, LOC111591502 +8 more	Copy number loss	See cases	GPathogenic
Select item 58863	GRCh38/hg38 7p21.1(chr7:18638299-18797297)x1	HDAC9	Copy number loss	See cases	GUncertain significance
Select item 58540	GRCh38/hg38 7p21.1(chr7:18931530-19221396)x1	FERD3L, HDAC9 +3 more	Copy number loss	See cases	GPathogenic
Select item 1230667	NM_178425.4(HDAC9):c.3023-91A>C	HDAC9	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar