Related gene-specific medical variations for Gene (Select 3127) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 149597	GRCh38/hg38 6p21.32(chr6:32489152-32571256)x3	HLA-DRB5	Copy number gain	See cases	GLikely benign
Select item 149444	GRCh38/hg38 6p21.32(chr6:32489152-32569033)x3	HLA-DRB5	Copy number gain	See cases	GLikely benign
Select item 147180	GRCh38/hg38 6p21.32(chr6:32482945-32554123)x3	HLA-DRB5	Copy number gain	See cases	GBenign
Select item 147101	GRCh38/hg38 6p21.32(chr6:32482945-32578707)x3	HLA-DRB5	Copy number gain	See cases	GBenign
Select item 147093	GRCh38/hg38 6p21.32(chr6:32482945-32558311)x3	HLA-DRB5	Copy number gain	See cases	GBenign
Select item 147064	GRCh38/hg38 6p21.32(chr6:32482945-32529554)x3	HLA-DRB5	Copy number gain	See cases	GBenign
Select item 147030	GRCh38/hg38 6p21.32(chr6:32489435-32554123)x1	HLA-DRB5	Copy number loss	See cases	GBenign

ClinVar