"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MTNR1A" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 644265	NC_000004.12:g.(?_185684754)_(186709827_?)del	CYP4V2, F11 +26 more	Deletion	not provided	GPathogenic
Select item 791529	NM_005958.4(MTNR1A):c.635T>C (p.Ile212Thr)	MTNR1A (I212T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 762676	NM_005958.4(MTNR1A):c.588C>T (p.Phe196=)	MTNR1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 716546	NM_005958.4(MTNR1A):c.470C>T (p.Ala157Val)	MTNR1A (A157V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3246717	NC_000004.11:g.(?_186064502)_(187630981_?)dup	ANKRD37, CCDC110 +15 more	Duplication	not provided	GUncertain significance
Select item 1433110	NC_000004.11:g.(?_186423448)_(187630981_?)dup	CYP4V2, F11 +7 more	Duplication	not provided	GUncertain significance
Select item 1374349	NC_000004.11:g.(?_186064527)_(187630981_?)del	ANKRD37, CCDC110 +15 more	Deletion	not provided	GPathogenic
Select item 1070873	NC_000004.11:g.(?_186997774)_(187630981_?)del	CYP4V2, F11 +5 more	Deletion	not provided	GPathogenic
Select item 831567	NC_000004.12:g.(?_186149141)_(186709827_?)del	CYP4V2, F11 +4 more	Deletion	not provided	GPathogenic

ClinVar