"ISCA site 4"[submitter] AND "SDK1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57453	GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3	ABCB5, ACTB +1298 more	Copy number gain	See cases	GPathogenic
Select item 149829	GRCh38/hg38 7p22.2(chr7:3383575-3657796)x3	SDK1	Copy number gain	See cases	GLikely benign
Select item 150949	GRCh38/hg38 7p22.2(chr7:3978187-4334459)x3	LOC105375131, LOC126859932 +2 more	Copy number gain	See cases	GLikely benign

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