"GeneDx"[submitter] AND "RASA3"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152621	GRCh37/hg19 13q34(chr13:114741757-114810347)x3	C13orf46, LOC126861873 +3 more	Copy number gain	See cases	GLikely benign
Select item 145831	GRCh37/hg19 13q34(chr13:114741757-114871923)x3	C13orf46, LOC126861873 +16 more	Copy number gain	See cases	GLikely benign
Select item 151251	GRCh37/hg19 13q34(chr13:114763851-114810347)x3	LOC126861873, LOC130010192 +2 more	Copy number gain	See cases	GLikely benign
Select item 145021	GRCh37/hg19 13q34(chr13:114781654-114893774)x3	LOC126861873, LOC126861874 +16 more	Copy number gain	See cases	GBenign
Select item 59924	GRCh38/hg38 13q32.3-34(chr13:100039860-114327173)x3	LOC132090158, LOC132090159 +395 more	Copy number gain	See cases	GPathogenic
Select item 152824	GRCh38/hg38 13q33.1-34(chr13:101762788-114340285)x3	LOC130010172, LOC130010173 +367 more	Copy number gain	See cases	GPathogenic
Select item 57685	GRCh38/hg38 13q33.1-34(chr13:102114025-114327173)x1	GAS6-AS1, GAS6-DT +363 more	Copy number loss	See cases	GPathogenic
Select item 57709	GRCh38/hg38 13q33.2-34(chr13:104461586-114327173)x1	ABHD13, ADPRHL1 +331 more	Copy number loss	See cases	GPathogenic
Select item 57710	GRCh38/hg38 13q33.2-34(chr13:104698508-114327173)x1	ABHD13, ADPRHL1 +331 more	Copy number loss	See cases	GPathogenic
Select item 253937	GRCh37/hg19 13q34(chr13:114768042-115092569)x1	CDC16, RASA3 +2 more	Copy number loss	See cases	GUncertain significance
Select item 253491	GRCh37/hg19 13q31.2-34(chr13:89796110-115083342)x1	ABCC4, ABHD13 +94 more	Copy number loss	See cases	GPathogenic
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic
Select item 58285	GRCh37/hg19 13q34(chr13:114739949-115085141)x3	CDC16, CHAMP1 +2 more	Copy number gain	See cases	GUncertain significance