"ISCA site 7"[submitter] AND "IGH"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 147073	GRCh38/hg38 14q32.33(chr14:106329925-106354331)x1	IGH, IGHV3-30 +2 more	Copy number loss	See cases	GBenign
Select item 147072	GRCh38/hg38 14q32.33(chr14:106329925-106354331)x3	IGH, IGHV3-30 +2 more	Copy number gain	See cases	GBenign
Select item 147110	GRCh38/hg38 14q32.33(chr14:106450803-106475159)x1	IGH, IGHV3-43	Copy number loss	See cases	GBenign
Select item 147155	GRCh37/hg19 14q32.33(chr14:106539719-106572277)x0	IGH	Copy number loss	See cases	GBenign
Select item 147007	GRCh37/hg19 14q32.33(chr14:106539719-106559073)x3	IGH	Copy number gain	See cases	GBenign
Select item 147006	GRCh37/hg19 14q32.33(chr14:106539719-106559073)x1	IGH	Copy number loss	See cases	GBenign
Select item 146950	GRCh37/hg19 14q32.33(chr14:106538451-106572278)x3	IGH	Copy number gain	See cases	GBenign

ClinVar