"GeneDx"[submitter] AND "BTRC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58777	GRCh38/hg38 10q23.33-24.32(chr10:93181201-101356779)x1	LOC130004555, LOC130004556 +375 more	Copy number loss	See cases	GPathogenic
Select item 59709	GRCh38/hg38 10q24.32(chr10:101253669-101395093)x3	BTRC, LINC02681 +5 more	Copy number gain	See cases	GPathogenic
Select item 144981	GRCh38/hg38 10q24.32(chr10:101261619-101468818)x3	BTRC, LINC02681 +4 more	Copy number gain	See cases	GUncertain significance
Select item 523913	NM_033637.4(BTRC):c.517A>T (p.Lys173Ter)	BTRC (K173* +2 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1222592	NM_033637.4(BTRC):c.556+7C>G	BTRC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253692	GRCh37/hg19 10q24.32(chr10:103208804-103431259)x3	FBXW4, DPCD +2 more	Copy number gain	See cases	GUncertain significance
Select item 253479	GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	ABLIM1, ABRAXAS2 +201 more	Copy number gain	See cases	GPathogenic

ClinVar