ClinVar for Gene (Select 100507351) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155275	GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3	AANAT, AATK +1013 more	Copy number gain	See cases	GPathogenic
Select item 60173	GRCh38/hg38 17q25.3(chr17:77320131-77564650)x3	LOC100507351, LOC112268198 +27 more	Copy number gain	See cases	GUncertain significance
Select item 58703	GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3	MIR636, MIR6516 +1033 more	Copy number gain	See cases	GPathogenic

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