ClinVar for Gene (Select 407032) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154460	GRCh38/hg38 6q12-14.2(chr6:64549655-83426791)x1	ADGRB3, ADGRB3-DT +310 more	Copy number loss	See cases	GPathogenic
Select item 154226	GRCh38/hg38 6q13(chr6:70794142-71972780)x3	B3GAT2, LINC00472 +18 more	Copy number gain	See cases	GUncertain significance
Select item 146273	GRCh38/hg38 6q13(chr6:70809191-71941709)x3	B3GAT2, LINC00472 +18 more	Copy number gain	See cases	GUncertain significance

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