"GeneDx"[submitter] AND "CYLD-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59468	GRCh38/hg38 16q11.2-12.1(chr16:46466829-51673196)x1	ABCC11, ABCC12 +202 more	Copy number loss	See cases	GPathogenic
Select item 59467	GRCh38/hg38 16q11.2-12.1(chr16:46466829-51939304)x1	ABCC11, ABCC12 +204 more	Copy number loss	See cases	GPathogenic
Select item 59486	GRCh38/hg38 16q11.2-12.1(chr16:46471520-52405956)x1	ABCC11, ABCC12 +209 more	Copy number loss	See cases	GPathogenic
Select item 59487	GRCh38/hg38 16q12.1-12.2(chr16:47250644-54121476)x1	ABCC11, ABCC12 +210 more	Copy number loss	See cases	GPathogenic
Select item 1225104	NC_000016.10:g.50741910G>T	CYLD, CYLD-AS1 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1244068	NC_000016.10:g.50741954G>C	CYLD, CYLD-AS1 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1274753	NM_001378743.1(CYLD):c.-204+132C>T	CYLD, CYLD-AS1 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar