CHL1-AS2[gene] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155626	GRCh38/hg38 3p26.3-26.2(chr3:20213-3244317)x1	CHL1, CHL1-AS1 +37 more	Copy number loss	See cases	GUncertain significance
Select item 154175	GRCh38/hg38 3p26.3-25.3(chr3:20213-9362037)x1	ARL8B, BHLHE40 +172 more	Copy number loss	See cases	GPathogenic
Select item 153284	GRCh38/hg38 3p26.3-25.3(chr3:20213-11221602)x1	ARL8B, ARPC4 +286 more	Copy number loss	See cases	GPathogenic
Select item 153221	GRCh38/hg38 3p26.3(chr3:20213-1755128)x1	CHL1, CHL1-AS1 +10 more	Copy number loss	See cases	GLikely benign
Select item 60014	GRCh38/hg38 3p26.3(chr3:20521-1209209)x1	CHL1, CHL1-AS1 +8 more	Copy number loss	See cases	GUncertain significance
Select item 155258	GRCh38/hg38 3p26.3-25.3(chr3:32241-10323124)x1	ARL8B, ARPC4 +263 more	Copy number loss	See cases	GPathogenic
Select item 155106	GRCh38/hg38 3p26.3-25.3(chr3:32241-10631310)x1	ARL8B, ARPC4 +271 more	Copy number loss	See cases	GPathogenic
Select item 152808	GRCh38/hg38 3p26.3-25.3(chr3:32241-8165256)x3	ARL8B, BHLHE40 +139 more	Copy number gain	See cases	GLikely pathogenic
Select item 152256	GRCh38/hg38 3p26.3-25.3(chr3:32241-9066287)x1	ARL8B, BHLHE40 +162 more	Copy number loss	See cases	GPathogenic
Select item 151534	GRCh38/hg38 3p26.3-25.3(chr3:32241-9574994)x1	ARL8B, BHLHE40 +184 more	Copy number loss	See cases	GPathogenic
Select item 150610	GRCh38/hg38 3p26.3-26.2(chr3:32241-3355776)x1	CHL1, CHL1-AS1 +36 more	Copy number loss	See cases	GLikely pathogenic
Select item 150393	GRCh38/hg38 3p26.3-25.3(chr3:32241-9469506)x1	ARL8B, BHLHE40 +181 more	Copy number loss	See cases	GPathogenic
Select item 150031	GRCh38/hg38 3p26.3-25.1(chr3:32241-13613818)x3	ARL8B, ARPC4 +406 more	Copy number gain	See cases	GPathogenic
Select item 149555	GRCh38/hg38 3p26.3-26.1(chr3:32241-6065999)x1	ARL8B, BHLHE40 +126 more	Copy number loss	See cases	GPathogenic
Select item 149331	GRCh38/hg38 3p26.3-25.3(chr3:32241-11379835)x1	ARL8B, ARPC4 +291 more	Copy number loss	See cases	GPathogenic
Select item 149236	GRCh38/hg38 3p26.3-26.1(chr3:32241-7056717)x1	LOC129936092, LOC129936093 +134 more	Copy number loss	See cases	GPathogenic
Select item 149085	GRCh38/hg38 3p26.3-25.2(chr3:32241-12681483)x1	ARL8B, ARPC4 +331 more	Copy number loss	See cases	GPathogenic
Select item 148946	GRCh38/hg38 3p26.3(chr3:32241-1798654)x1	CHL1, CHL1-AS1 +10 more	Copy number loss	See cases	GUncertain significance
Select item 148942	GRCh38/hg38 3p26.3-24.1(chr3:32241-30064208)x3	ANKRD28, ARL8B +799 more	Copy number gain	See cases	GPathogenic
Select item 148876	GRCh38/hg38 3p26.3-24.3(chr3:32241-20334387)x3	LOC129936198, LOC129936199 +647 more	Copy number gain	See cases	GPathogenic
Select item 144853	GRCh38/hg38 3p26.3-26.1(chr3:32241-5791120)x1	ARL8B, BHLHE40 +126 more	Copy number loss	See cases	GPathogenic
Select item 154669	GRCh38/hg38 3p26.3-26.1(chr3:52266-4827490)x1	CHL1, CHL1-AS1 +72 more	Copy number loss	See cases	GPathogenic
Select item 154516	GRCh38/hg38 3p26.3(chr3:52266-1091944)x1	CHL1, CHL1-AS1 +6 more	Copy number loss	See cases	GUncertain significance
Select item 154452	GRCh38/hg38 3p26.3-26.1(chr3:52266-5966084)x3	ARL8B, BHLHE40 +126 more	Copy number gain	See cases	GPathogenic
Select item 148015	GRCh38/hg38 3p26.3-25.3(chr3:52266-9450310)x1	ARL8B, BHLHE40 +181 more	Copy number loss	See cases	GPathogenic
Select item 147496	GRCh38/hg38 3p26.3-26.1(chr3:52266-6277604)x1	ARL8B, BHLHE40 +126 more	Copy number loss	See cases	GPathogenic
Select item 146281	GRCh38/hg38 3p26.3-26.1(chr3:52266-5138262)x1	ARL8B, BHLHE40 +102 more	Copy number loss	See cases	GPathogenic
Select item 145577	GRCh38/hg38 3p26.3(chr3:52266-868393)x3	CHL1, CHL1-AS1 +6 more	Copy number gain	See cases	GPathogenic
Select item 57734	GRCh38/hg38 3p26.3-25.3(chr3:52266-8582037)x1	ARL8B, BHLHE40 +144 more	Copy number loss	See cases	GPathogenic
Select item 57708	GRCh38/hg38 3p26.3-25.3(chr3:52266-11089569)x1	ARL8B, ARPC4 +281 more	Copy number loss	See cases	GPathogenic
Select item 57397	GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3	LOC129936421, LOC129936422 +962 more	Copy number gain	See cases	GPathogenic
Select item 150281	GRCh38/hg38 3p26.3-25.3(chr3:52747-8370373)x1	ARL8B, BHLHE40 +141 more	Copy number loss	See cases	GPathogenic
Select item 153415	GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3	ACAA1, ACVR2B +1111 more	Copy number gain	See cases	GPathogenic
Select item 545299	Single allele	CHL1, CHL1-AS1 +14 more	Duplication	Autism	GLikely pathogenic
Select item 59098	GRCh38/hg38 3p26.3(chr3:63843-325628)x3	CHL1, CHL1-AS2 +3 more	Copy number gain	See cases	GUncertain significance
Select item 59097	GRCh38/hg38 3p26.3(chr3:63843-1209209)x3	CHL1, CHL1-AS1 +7 more	Copy number gain	See cases	GUncertain significance
Select item 57977	GRCh38/hg38 3p26.3-24.3(chr3:63843-19510600)x3	LOC110120630, LOC111429626 +608 more	Copy number gain	See cases	GPathogenic
Select item 57738	GRCh38/hg38 3p26.3-25.3(chr3:63843-8258109)x1	ARL8B, BHLHE40 +140 more	Copy number loss	See cases	GPathogenic
Select item 57737	GRCh38/hg38 3p26.3-26.1(chr3:63843-4708786)x1	CHL1, CHL1-AS1 +66 more	Copy number loss	See cases	GPathogenic
Select item 57736	GRCh38/hg38 3p26.3-25.3(chr3:63843-9507969)x1	ARL8B, BHLHE40 +184 more	Copy number loss	See cases	GPathogenic
Select item 57735	GRCh38/hg38 3p26.3-26.1(chr3:63843-6977502)x1	ARL8B, BHLHE40 +134 more	Copy number loss	See cases	GPathogenic
Select item 56999	GRCh38/hg38 3p26.3(chr3:76052-229025)x1	CHL1, CHL1-AS2 +2 more	Copy number loss	See cases	GUncertain significance
Select item 144856	GRCh38/hg38 3p26.3(chr3:85837-296216)x3	CHL1, CHL1-AS2 +2 more	Copy number gain	See cases	GBenign
Select item 154038	GRCh38/hg38 3p26.3(chr3:144528-713567)x3	CHL1, CHL1-AS1 +3 more	Copy number gain	See cases	GLikely benign
Select item 60015	GRCh38/hg38 3p26.3(chr3:171028-1018461)x1	CHL1, CHL1-AS1 +4 more	Copy number loss	See cases	GUncertain significance
Select item 155072	GRCh38/hg38 3p26.3(chr3:182931-937659)x3	CHL1, CHL1-AS1 +4 more	Copy number gain	See cases	GLikely benign
Select item 154557	GRCh38/hg38 3p26.3(chr3:190587-608819)x1	CHL1, CHL1-AS1 +3 more	Copy number loss	See cases	GUncertain significance
Select item 151881	GRCh38/hg38 3p26.3(chr3:190813-213696)x3	CHL1, CHL1-AS2	Copy number gain	See cases	GBenign
Select item 146345	GRCh38/hg38 3p26.3(chr3:190813-2045586)x3	CHL1, CHL1-AS1 +8 more	Copy number gain	See cases	GUncertain significance
Select item 144261	GRCh38/hg38 3p26.3(chr3:190813-1155998)x1	CHL1, CHL1-AS1 +5 more	Copy number loss	See cases	GUncertain significance

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Items: 50