ClinVar for Gene (Select 5558) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809510	GRCh38/hg38 6p12.1-11.2(chr6:55755662-55874865)x2	LINC01564, LINC03001 +88 more	Copy number loss	Orofacial cleft	GUncertain significance
Select item 153981	GRCh38/hg38 6p11.2-q11.1(chr6:57447932-60420111)x1	LINC00680, LOC101927293 +10 more	Copy number loss	See cases	GLikely benign
Select item 151123	GRCh38/hg38 6p11.2-q11.1(chr6:57436696-60420111)x3	LINC00680, LOC101927293 +10 more	Copy number gain	See cases	GLikely benign
Select item 148991	GRCh38/hg38 6p11.2-q12(chr6:57466921-68712228)x3	ADGRB3, ADGRB3-DT +105 more	Copy number gain	See cases	GPathogenic
Select item 148002	GRCh38/hg38 6p12.1-q12(chr6:53931543-68149750)x3	BAG2, BEND6 +147 more	Copy number gain	See cases	GPathogenic
Select item 146506	GRCh38/hg38 6p12.1-11.2(chr6:56639682-57432788)x3	BAG2, BEND6 +27 more	Copy number gain	See cases	GUncertain significance
Select item 145584	GRCh38/hg38 6p12.3-11.2(chr6:50971182-57432788)x1	BAG2, BEND6 +171 more	Copy number loss	See cases	GPathogenic
Select item 144369	GRCh38/hg38 6p12.1-11.2(chr6:56312924-57306212)x1	BAG2, BEND6 +28 more	Copy number loss	See cases	GUncertain significance

ClinVar