LOC110121298[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CCDC146, CCDC201 +4735 more	Copy number loss	See cases	GPathogenic
Select item 154461	GRCh38/hg38 7q11.21-11.23(chr7:62736364-75432710)x1	LOC129998532, LOC129998533 +350 more	Copy number loss	See cases	GPathogenic
Select item 154104	GRCh38/hg38 7q11.21-11.23(chr7:62977085-75415352)x3	LOC129998632, LOC129998633 +349 more	Copy number gain	See cases	GPathogenic
Select item 57022	GRCh38/hg38 7q11.21-11.22(chr7:64657050-72243063)x1	ASL, AUTS2 +157 more	Copy number loss	See cases	GPathogenic
Select item 58552	GRCh38/hg38 7q11.22-11.23(chr7:68668307-73710276)x1	AUTS2, BAZ1B +117 more	Copy number loss	See cases	GPathogenic
Select item 144764	GRCh38/hg38 7q11.22(chr7:69000832-70244446)x1	AUTS2, CT66 +24 more	Copy number loss	See cases	GPathogenic
Select item 60237	GRCh38/hg38 7q11.22-11.23(chr7:69382353-77823832)x1	SPDYE12, SPDYE13 +330 more	Copy number loss	See cases	GPathogenic
Select item 148274	GRCh38/hg38 7q11.22(chr7:69665251-70271848)x1	AUTS2, LOC108004522 +15 more	Copy number loss	See cases	GPathogenic
Select item 133343	NC_000007.14:g.(69899499_70118132)_(70134571_70435751)del	AUTS2, LOC108004522 +8 more	Deletion	Autism spectrum disorder due to AUTS2 deficiency	GPathogenic
Select item 154881	GRCh38/hg38 7q11.22(chr7:70055626-70319823)x1	AUTS2, LOC108004522 +6 more	Copy number loss	See cases	GUncertain significance