"GeneDx"[submitter] AND "LOC129388446"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59884	GRCh38/hg38 1p36.23-36.21(chr1:7165036-13111056)x1	AADACL3, AADACL4 +386 more	Copy number loss	See cases	GPathogenic
Select item 59885	GRCh38/hg38 1p36.23-36.13(chr1:9034671-16441465)x1	AADACL3, AADACL4 +462 more	Copy number loss	See cases	GPathogenic
Select item 1251192	NM_001365951.3(KIF1B):c.-26TA[5]	KIF1B, LOC129388446	Microsatellite (5 prime UTR variant)	not provided	GBenign

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