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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59821	GRCh38/hg38 12q24.21-24.33(chr12:115131583-133166920)x3	LOC130009192, LOC130009193 +892 more	Copy number gain	See cases	GPathogenic
Select item 1294746	NM_176818.3(GATC):c.8C>T (p.Ser3Leu)	GATC, LOC112163529 (S3L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1246559	NM_176818.3(GATC):c.45C>T (p.Gly15=)	GATC, LOC112163529	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1263252	NM_176818.3(GATC):c.255-194C>T	GATC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 429332	NM_176818.3(GATC):c.310C>G (p.Leu104Val)	GATC (L104V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1182274	NM_176818.3(GATC):c.359-151C>T	GATC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239885	NM_176818.3(GATC):c.359-58T>C	GATC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236331	NM_176818.3(GATC):c.*10T>G	GATC	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

ClinVar