Related gene-specific medical variations for Gene (Select 55100) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685156	GRCh37/hg19 5p13.2(chr5:37448370-37778559)x1	WDR70	Copy number loss	not provided	GUncertain significance
Select item 2242700	NM_018034.4(WDR70):c.1634G>A (p.Arg545Gln)	LOC126807364, WDR70 (R544Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340951	GRCh37/hg19 5p13.2(chr5:37414308-37480597)x1	WDR70	Copy number loss	not provided	GLikely benign
Select item 1340504	GRCh37/hg19 5p13.2(chr5:37382795-37472715)x1	WDR70	Copy number loss	not provided	GLikely benign
Select item 814683	GRCh37/hg19 5p13.2(chr5:37373774-37753977)x3	WDR70	Copy number gain	not provided	GUncertain significance
Select item 563058	GRCh37/hg19 5p13.2(chr5:37468349-37585849)x1	WDR70	Copy number loss	not provided	GUncertain significance
Select item 563057	GRCh37/hg19 5p13.2(chr5:37376949-37561791)x1	WDR70	Copy number loss	not provided	GUncertain significance

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