"GeneDx"[submitter] AND "ARHGAP26"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 146046	GRCh38/hg38 5q31.3(chr5:142643032-142900779)x3	ARHGAP26, ARHGAP26-AS1 +12 more	Copy number gain	See cases	GUncertain significance
Select item 152431	GRCh38/hg38 5q31.3(chr5:143198264-143252477)x3	ARHGAP26, LOC129994904 +6 more	Copy number gain	See cases	GUncertain significance
Select item 1250331	NM_001135608.3(ARHGAP26):c.*3558C>T	ARHGAP26	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

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