ClinVar (all) for Orgtrack (Select 506987) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 805869	NM_004409.4:c.224_283CTG[(271_852)]CCG[1]CTG[17]CCG[1]CTG[29]	DMPK	Microsatellite	Steinert myotonic dystrophy syndrome	GPathogenic
Select item 805868	NM_004409.4:c.224_283CTG[(510_860)]CCG[1]CTG[1]CCG[1]CTG[1]CCG[1]CTG[2]CCG[3]CTG[1]CCG[1]CTG[4]CCG[1]CTG[1]CCG[1]CTG[18]	DMPK	Microsatellite	Steinert myotonic dystrophy syndrome	GPathogenic
Select item 805867	NM_004409.4:c.224_283CTG[329]NNN[(?)]CCG[1]CTG[1]CCG[1]CTG[1]CCG[1]CTG[4]CCG[1]CTG[1]CCG[1]CTG[1]CCG[1]CTG[4]CCG[1]CTG[1]CCG[1]CTG[18]	DMPK	Microsatellite	Steinert myotonic dystrophy syndrome	GPathogenic
Select item 805866	NM_004409.4:c.224_283CTG[(192_602)]CCG[1]CTG[8]CCG[2]CTG[2]CCG[1]CTG[4]CCG[1]CTG[30]	DMPK	Microsatellite	Steinert myotonic dystrophy syndrome	GPathogenic
Select item 805865	NM_004409.4:c.*224CTG[173_283]CCG[1]CTG[8]CCG[2]CTG[2]CCG[1]CTG[4]CCG[1]CTG[30]	DMPK	Microsatellite	Steinert myotonic dystrophy syndrome	GLikely pathogenic

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