"GeneDx"[submitter] AND "ZNF804A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58770	GRCh38/hg38 2q31.1-33.1(chr2:176304445-202039790)x1	LOC126806416, LOC126806417 +591 more	Copy number loss	See cases	GPathogenic
Select item 58771	GRCh38/hg38 2q31.2-33.1(chr2:177874070-198525492)x1	ANKAR, ANKRD44 +430 more	Copy number loss	See cases	GPathogenic
Select item 58772	GRCh38/hg38 2q31.2-32.1(chr2:178880151-185352829)x1	CCDC141, CERKL +104 more	Copy number loss	See cases	GPathogenic
Select item 59883	GRCh38/hg38 2q32.1(chr2:184482607-185243974)x1	LOC105373780, LOC105373782 +3 more	Copy number loss	See cases	GBenign
Select item 145833	GRCh38/hg38 2q32.1(chr2:184499992-185229822)x1	LOC105373780, LOC105373782 +3 more	Copy number loss	See cases	GLikely benign
Select item 1221151	NM_194250.2(ZNF804A):c.782A>T (p.Gln261Leu)	ZNF804A (Q261L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1280392	NM_194250.2(ZNF804A):c.3241C>G (p.Leu1081Val)	ZNF804A (L1081V)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar