"GeneDx"[submitter] AND "IL21"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	LOC129993082, LOC129993083 +661 more	Copy number gain	See cases	GPathogenic
Select item 1269619	NM_021803.4(IL21):c.*45G>A	IL21	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1229892	NM_021803.4(IL21):c.*31C>T	IL21	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1237452	NM_021803.4(IL21):c.361-330T>C	IL21	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222331	NM_021803.4(IL21):c.360+139dup	IL21	Duplication (intron variant)	not provided	GBenign
Select item 1235132	NM_021803.4(IL21):c.360+150_360+154del	IL21	Deletion (intron variant)	not provided	GBenign
Select item 402975	NM_021803.4(IL21):c.234C>T (p.Cys78=)	IL21	Single nucleotide variant (synonymous variant)	IL21-related infantile inflammatory bowel disease +2 more	GBenign
Select item 253606	GRCh37/hg19 4q26-35.2(chr4:119437495-190904301)x3	SCOC, SCRG1 +218 more	Copy number gain	See cases	GPathogenic

ClinVar