ClinVar for Gene (Select 126863009) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 545233	NC_000020.11:g.(?_25564868)_(25611357_?)del	LOC125387247, LOC126863009 +2 more	Deletion	Autism	GLikely pathogenic
Select item 155473	GRCh38/hg38 20p11.21(chr20:25031679-25625520)x3	ABHD12, ACSS1 +45 more	Copy number gain	See cases	GUncertain significance
Select item 153731	GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3	MIR6869, MIR6870 +828 more	Copy number gain	See cases	GPathogenic
Select item 152985	GRCh38/hg38 20p11.21(chr20:25485770-25612650)x3	LOC121627901, LOC125387247 +3 more	Copy number gain	See cases	GBenign
Select item 148112	GRCh38/hg38 20p11.21(chr20:25485770-25612660)x3	LOC121627901, LOC125387247 +3 more	Copy number gain	See cases	GBenign
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	LOC130065566, LOC130065567 +2522 more	Copy number gain	See cases	GPathogenic
Select item 144514	GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3	LOC111365169, LOC111365189 +833 more	Copy number gain	See cases	GPathogenic
Select item 59196	GRCh38/hg38 20p11.22-q11.1(chr20:22061586-30285812)x3	ABHD12, ACSS1 +174 more	Copy number gain	See cases	GPathogenic
Select item 59195	GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	LOC130065574, LOC130065575 +950 more	Copy number gain	See cases	GPathogenic
Select item 57514	GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3	LOC126862999, LOC126863005 +814 more	Copy number gain	See cases	GPathogenic