"GeneDx"[submitter] AND "SLIT1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58776	GRCh38/hg38 10q23.33-24.2(chr10:92626680-97755102)x1	LOC105378448, LOC107195252 +245 more	Copy number loss	See cases	GPathogenic
Select item 58777	GRCh38/hg38 10q23.33-24.32(chr10:93181201-101356779)x1	LOC130004555, LOC130004556 +375 more	Copy number loss	See cases	GPathogenic
Select item 768381	NM_003061.3(SLIT1):c.1431C>A (p.Ile477=)	SLIT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1241884	NM_003061.3(SLIT1):c.1311G>C (p.Ala437=)	SLIT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 152653	GRCh38/hg38 10q24.1(chr10:97123320-97197359)x3	ARHGAP19-SLIT1, LOC129390219 +5 more	Copy number gain	See cases	GLikely benign
Select item 253819	GRCh37/hg19 10q24.1(chr10:98941691-99153357)x3	FRAT1, FRAT2 +3 more	Copy number gain	See cases	GUncertain significance

ClinVar