"GeneDx"[submitter] AND "GPR68"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58526	GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3	LOC130056392, LOC130056393 +1073 more	Copy number gain	See cases	GPathogenic
Select item 57811	GRCh38/hg38 14q32.11-32.13(chr14:90255156-95274696)x1	ASB2, ATXN3 +201 more	Copy number loss	See cases	GPathogenic
Select item 58334	GRCh38/hg38 14q32.11(chr14:90495001-91296461)x3	CCDC88C, DGLUCY +45 more	Copy number gain	See cases	GUncertain significance
Select item 1286992	NM_001177676.2(GPR68):c.549C>T (p.Arg183=)	GPR68	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1181225	NM_001177676.2(GPR68):c.114C>T (p.Ala38=)	GPR68	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1274562	NM_001177676.2(GPR68):c.-129-305TTAT[11]	GPR68	Microsatellite (intron variant)	not provided	GBenign
Select item 1269278	NM_001177676.2(GPR68):c.-129-305TTAT[9]	GPR68	Microsatellite (intron variant)	not provided	GBenign
Select item 1263752	NM_001177676.2(GPR68):c.-129-305TTAT[10]	GPR68	Microsatellite (intron variant)	not provided	GBenign
Select item 1241549	NM_001177676.2(GPR68):c.-129-305TTAT[7]	GPR68	Microsatellite (intron variant)	not provided	GBenign
Select item 1260988	NM_001177676.2(GPR68):c.-129-264T>A	GPR68	Single nucleotide variant (intron variant)	not provided	GBenign