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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58552	GRCh38/hg38 7q11.22-11.23(chr7:68668307-73710276)x1	AUTS2, BAZ1B +117 more	Copy number loss	See cases	GPathogenic
Select item 60237	GRCh38/hg38 7q11.22-11.23(chr7:69382353-77823832)x1	SPDYE12, SPDYE13 +330 more	Copy number loss	See cases	GPathogenic
Select item 1277241	NM_032951.3(MLXIPL):c.*589A>G	MLXIPL	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 253635	GRCh37/hg19 7q11.22-11.23(chr7:71968212-74133332)x3	CLDN4, POM121 +28 more	Copy number gain	See cases	GPathogenic
Select item 253539	GRCh37/hg19 7q11.23(chr7:72718252-74133332)x1	LAT2, GTF2IRD1 +25 more	Copy number loss	See cases	GPathogenic
Select item 253423	GRCh37/hg19 7q11.23(chr7:72708237-74339044)x1	VPS37D, CLIP2 +27 more	Copy number loss	See cases	GPathogenic

ClinVar