ClinVar for Gene (Select 100874008) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1279233	NC_000003.12:g.55487689C>A	WNT5A, WNT5A-AS1	Single nucleotide variant (genic upstream transcript variant)	not provided	GBenign
Select item 1262259	NC_000003.12:g.55487931dup	WNT5A, WNT5A-AS1	Duplication (genic upstream transcript variant)	not provided	GBenign
Select item 1187730	NC_000003.12:g.55487694C>A	WNT5A, WNT5A-AS1	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1183525	NC_000003.12:g.55487693G>A	WNT5A, WNT5A-AS1	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 60057	GRCh38/hg38 3p21.1-14.3(chr3:53287477-57025368)x1	ACTR8, ARHGEF3 +53 more	Copy number loss	See cases	GUncertain significance
Select item 57386	GRCh38/hg38 3p21.1-14.1(chr3:54045018-66060461)x1	ABHD6, ACOX2 +217 more	Copy number loss	See cases	GPathogenic

ClinVar