"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PTPRG-AS1" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3025815	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 3024706	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653933	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653932	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653931	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653930	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653929	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653928	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign

ClinVar