LOC106780804[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	LOC110121220, LOC110121246 +2579 more	Copy number gain	See cases	GPathogenic
Select item 153079	GRCh38/hg38 6p21.33(chr6:31971993-32012974)x1	C4A, DXO +3 more	Copy number loss	See cases	GBenign
Select item 150716	GRCh38/hg38 6p21.33(chr6:31980353-32041234)x3	C4A, C4B +7 more	Copy number gain	See cases	GLikely benign
Select item 152997	GRCh38/hg38 6p21.33(chr6:31980422-32041505)x1	C4A, C4B +7 more	Copy number loss	See cases	GBenign
Select item 154968	GRCh38/hg38 6p21.33(chr6:31996044-32041234)x3	C4A, C4B +6 more	Copy number gain	See cases	GLikely benign
Select item 154793	GRCh38/hg38 6p21.33(chr6:31996044-32040430)x1	C4A, C4B +5 more	Copy number loss	See cases	GLikely benign
Select item 154792	GRCh38/hg38 6p21.33(chr6:31996044-32040430)x3	C4A, C4B +5 more	Copy number gain	See cases	GLikely benign
Select item 149713	GRCh38/hg38 6p21.33(chr6:31996044-32040241)x3	C4A, C4B +5 more	Copy number gain	See cases	GLikely benign
Select item 147011	GRCh38/hg38 6p21.33(chr6:31996089-32041483)x1	C4A, C4B +6 more	Copy number loss	See cases	GBenign

ClinVar