ClinVar for Gene (Select 475) - ClinVar - NCBI

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Links from Gene

Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327258	NM_004045.4(ATOX1):c.102C>A (p.Asp34Glu)	ATOX1 (D34E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3246326	NC_000005.9:g.(?_150632778)_(151304110_?)dup	ATOX1, FAT2 +7 more	Duplication	Hereditary hyperekplexia	GUncertain significance
Select item 3131211	NM_004045.4(ATOX1):c.76C>T (p.Leu26Phe)	ATOX1 (L26F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131210	NM_004045.4(ATOX1):c.167A>G (p.Lys56Arg)	ATOX1 (K56R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2424627	NC_000005.9:g.(?_150885126)_(151304110_?)dup	GLRA1, ATOX1 +3 more	Duplication	not provided	GUncertain significance
Select item 2331898	NM_004045.4(ATOX1):c.149C>A (p.Thr50Asn)	ATOX1 (T50N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808662	GRCh37/hg19 5q33.1-35.2(chr5:150535183-172906793)x3	ADAM19, ADRA1B +98 more	Copy number gain	not provided	GPathogenic
Select item 1703528	GRCh37/hg19 5q32-35.3(chr5:149010383-180719789)	ADAM19, ADAMTS2 +222 more	Copy number gain	Hunter-McAlpine craniosynostosis	GPathogenic
Select item 457359	NC_000005.9:g.(?_86400000)_(154000000_?)del	CCDC69, CCNH +385 more	Deletion	Familial adenomatous polyposis 1 +1 more	GPathogenic
Select item 442431	GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	DHFR, DHX29 +738 more	Copy number loss	See cases	GPathogenic
Select item 441920	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 441919	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign
Select item 394550	GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3	HRH2, HSD17B4 +520 more	Copy number gain	See cases	GPathogenic
Select item 149858	GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3	LOC129994992, LOC129994993 +1157 more	Copy number gain	See cases	GPathogenic
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 58118	GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3	LOC132089226, LOC132089227 +1167 more	Copy number gain	See cases	GPathogenic
Select item 57483	GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3	ABLIM3, ACSL6 +1218 more	Copy number gain	See cases	GPathogenic