103504738[Gene ID] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151635	GRCh38/hg38 16p13.3(chr16:16203-129081)x3	HBA-LCR, LOC121530606 +14 more	Copy number gain	See cases	GBenign
Select item 145276	GRCh38/hg38 16p13.3(chr16:16203-32412)x1	MIR6859-4, WASIR2	Copy number loss	See cases	GBenign
Select item 145275	GRCh38/hg38 16p13.3(chr16:16203-32412)x3	MIR6859-4, WASIR2	Copy number gain	See cases	GBenign/Likely benign

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