ASNS[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3245931	NC_000007.13:g.(?_97493753)_(97495499_?)del	ASNS	Deletion	not provided	GLikely pathogenic
Select item 2427214	NC_000007.13:g.(?_97488515)_(97493818_?)del	ASNS	Deletion	not provided	GPathogenic
Select item 1457009	NC_000007.13:g.(?_97498200)_(97498468_?)del	ASNS	Deletion	not provided	GPathogenic
Select item 1457008	NC_000007.13:g.(?_97481561)_(97498478_?)del	ASNS	Deletion	not provided	GPathogenic
Select item 1412691	NC_000007.13:g.(?_97481571)_(97498468_?)dup	ASNS	Duplication	not provided	GUncertain significance
Select item 1676433	NC_000007.14:g.97859375C>T	ASNS (A150T +2 more)	Single nucleotide variant	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar