ClinVar for Gene (Select 101929210) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2579270	GRCh38/hg38 4q21.21-23(chr4:79123548-99457773)x1	ABCG2, ABRAXAS1 +338 more	Copy number loss	Chromosome 4q21 deletion syndrome	GPathogenic
Select item 1050853	Single allele	LOC129992843, SMARCAD1 +1 more	Complex	Basan syndrome	GPathogenic
Select item 155391	GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3	LOC129992695, LOC129992696 +533 more	Copy number gain	See cases	GPathogenic
Select item 155131	GRCh38/hg38 4q22.2-22.3(chr4:93368807-94200572)x1	ATOH1, GRID2 +7 more	Copy number loss	See cases	GUncertain significance
Select item 152885	GRCh38/hg38 4q22.2-22.3(chr4:94071164-94561427)x4	HPGDS, LOC112997547 +7 more	Copy number gain	See cases	GUncertain significance
Select item 151714	GRCh38/hg38 4q22.1-24(chr4:92610413-101521991)x1	ADH1A, ADH1B +123 more	Copy number loss	See cases	GPathogenic
Select item 148666	GRCh38/hg38 4q22.1-22.3(chr4:92087558-94308725)x1	ATOH1, GRID2 +14 more	Copy number loss	See cases	GUncertain significance
Select item 148194	GRCh38/hg38 4q21.21-24(chr4:80427023-100855441)x1	ABCG2, ABRAXAS1 +335 more	Copy number loss	See cases	GPathogenic
Select item 145649	GRCh38/hg38 4q21.21-22.3(chr4:80879777-94809447)x1	ABCG2, ABRAXAS1 +244 more	Copy number loss	See cases	GPathogenic
Select item 58029	GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	LOC129389216, LOC129389217 +757 more	Copy number gain	See cases	GPathogenic