"GeneDx"[submitter] AND "IL37"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152532	GRCh38/hg38 2q14.1(chr2:112878355-113035551)x3	IL36A, IL36B +9 more	Copy number gain	See cases	GLikely benign
Select item 767816	NM_014439.4(IL37):c.124A>G (p.Thr42Ala)	IL37 (T42A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 253673	GRCh37/hg19 2q12.2-14.1(chr2:106423310-115054828)x1	BUB1, PSD4 +53 more	Copy number loss	See cases	GPathogenic
Select item 253541	GRCh37/hg19 2q12.3-14.1(chr2:109556627-117570152)x1	TMEM87B, IL37 +40 more	Copy number loss	See cases	GPathogenic
Select item 253388	GRCh37/hg19 2q12.3-14.3(chr2:109798247-125658380)x1	RGPD8, ACTR3 +63 more	Copy number loss	See cases	GPathogenic

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