"GeneDx"[submitter] AND "BCR"[gene] - ClinVar - NCBI

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Search results

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146012	GRCh38/hg38 22q11.22-11.23(chr22:22669543-23300977)x3	BCR, GNAZ +80 more	Copy number gain	See cases	GPathogenic
Select item 59039	GRCh38/hg38 22q11.23(chr22:23247480-23670363)x3	BCR, DRICH1 +21 more	Copy number gain	See cases	GUncertain significance
Select item 1182413	NM_004327.4(BCR):c.2387A>G (p.Asn796Ser)	BCR (N796S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 769154	NM_004327.4(BCR):c.3183-4G>A	BCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253528	GRCh37/hg19 22q11.21-11.23(chr22:20749625-23972878)x1	AIFM3, BCR +40 more	Copy number loss	See cases	GPathogenic
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 253499	GRCh37/hg19 22q11.22-11.23(chr22:22988879-24276233)x3	CHCHD10, RAB36 +17 more	Copy number gain	See cases	GPathogenic
Select item 253485	GRCh37/hg19 22q11.22-11.23(chr22:22976696-25053311)x3	GSTT2B, VPREB3 +32 more	Copy number gain	See cases	GPathogenic
Select item 253473	GRCh37/hg19 22q11.1-12.1(chr22:16054691-27296513)x3	ADA2, ADORA2A +135 more	Copy number gain	See cases	GPathogenic
Select item 253435	GRCh37/hg19 22q11.22-11.23(chr22:23258229-25046803)x3	RSPH14, SNRPD3 +29 more	Copy number gain	See cases	GPathogenic
Select item 253433	GRCh37/hg19 22q11.21-11.23(chr22:21400683-23654222)x3	BCR, CCDC116 +25 more	Copy number gain	See cases	GPathogenic
Select item 253351	GRCh37/hg19 22q11.22-11.23(chr22:23258229-23654222)x1	RAB36, GNAZ +2 more	Copy number loss	See cases	GLikely pathogenic