ClinVar for Gene (Select 1875) - ClinVar

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Links from Gene

Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086750	NM_001951.4(E2F5):c.92A>G (p.Gln31Arg)	E2F5, LOC130000687 (Q31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086749	NM_001951.4(E2F5):c.853C>A (p.Gln285Lys)	E2F5 (Q124K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086748	NM_001951.4(E2F5):c.827A>C (p.His276Pro)	E2F5 (H276P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086747	NM_001951.4(E2F5):c.694G>C (p.Glu232Gln)	E2F5 (E232Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086746	NM_001951.4(E2F5):c.139G>A (p.Gly47Ser)	E2F5, LOC130000687 (G47S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063037	GRCh37/hg19 8q21.2-21.3(chr8:85339090-89534521)x3	ATP6V0D2, CA1 +16 more	Copy number gain	not specified	GUncertain significance
Select item 3063025	GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	ADAM18, ADAM2 +240 more	Copy number gain	not specified	GPathogenic
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 2685315	GRCh37/hg19 8q21.13-22.1(chr8:84127576-98263585)x1	ATP6V0D2, CA1 +53 more	Copy number loss	not provided	GPathogenic
Select item 2684547	GRCh37/hg19 8q21.2(chr8:86060380-86553118)x3	CA1, CA13 +4 more	Copy number gain	not provided	GUncertain significance
Select item 2684546	GRCh37/hg19 8q21.12-22.3(chr8:79046933-102008860)x3	ANKRD46, ATP6V0D2 +96 more	Copy number gain	not provided	GPathogenic
Select item 2606519	NM_001951.4(E2F5):c.470G>A (p.Ser157Asn)	E2F5 (S157N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545448	NM_001951.4(E2F5):c.243T>A (p.Asp81Glu)	E2F5 (D81E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531295	NM_001951.4(E2F5):c.211G>A (p.Asp71Asn)	E2F5, LOC130000688 (D71N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2426512	NC_000008.10:g.(?_86053597)_(87755855_?)dup	CA3, CA2 +12 more	Duplication	not provided	GUncertain significance
Select item 2361092	NM_001951.4(E2F5):c.549T>A (p.Asn183Lys)	E2F5 (N22K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316148	NM_001951.4(E2F5):c.124G>A (p.Gly42Arg)	E2F5, LOC130000687 (G42R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288866	NM_001951.4(E2F5):c.574G>T (p.Ala192Ser)	E2F5 (A31S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285386	NM_001951.4(E2F5):c.233C>A (p.Ala78Glu)	E2F5, LOC130000688 (A78E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277850	NM_001951.4(E2F5):c.531C>A (p.Asp177Glu)	E2F5 (D16E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276425	NM_001951.4(E2F5):c.974A>T (p.Tyr325Phe)	E2F5 (Y164F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270148	NM_001951.4(E2F5):c.621G>C (p.Gln207His)	E2F5 (Q46H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251714	NM_001951.4(E2F5):c.381A>G (p.Ile127Met)	E2F5 (I127M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234665	NM_001951.4(E2F5):c.903T>A (p.Asp301Glu)	E2F5 (D140E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809213	GRCh37/hg19 8q21.13-21.2(chr8:83705217-86441492)x1	CA1, CA13 +6 more	Copy number loss	not provided	GUncertain significance
Select item 1808681	GRCh37/hg19 8q21.12-24.11(chr8:79409349-119040631)x3	AARD, ABRA +141 more	Copy number gain	not provided	GPathogenic
Select item 1711167	GRCh37/hg19 8q13.2-24.3(chr8:68912432-146295771)x2	AARD, ABRA +335 more	Copy number gain	See cases	GPathogenic
Select item 1706511	GRCh37/hg19 8q21.2-24.3(chr8:84712253-146295771)x3	AARD, ABRA +285 more	Copy number gain	See cases	GPathogenic
Select item 1703544	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	AARD, ABRA +665 more	Copy number gain	Polydactyly	GPathogenic
Select item 1527444	GRCh37/hg19 8q21.11-21.3(chr8:77906471-88917707)	ATP6V0D2, CA1 +36 more	Copy number loss	not specified	GPathogenic
Select item 1527440	GRCh37/hg19 8q13.2-24.3(chr8:70382990-146295771)	DCAF4L2, DCSTAMP +333 more	Copy number gain	not specified	GPathogenic
Select item 1341980	GRCh37/hg19 8q21.11-21.3(chr8:75904944-87097083)x1	CA1, CA13 +31 more	Copy number loss	Chromosome 8q21.11 deletion syndrome	GPathogenic
Select item 815141	GRCh37/hg19 8q21.2(chr8:85635587-86553130)x3	CA3, CA1 +6 more	Copy number gain	not provided	GUncertain significance
Select item 815140	GRCh37/hg19 8q21.13-21.2(chr8:83541683-86091081)x3	RALYL, E2F5 +1 more	Copy number gain	not provided	GLikely benign
Select item 687787	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	MICU3, MIR1234 +665 more	Copy number gain	not provided	GPathogenic
Select item 687493	GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	VPS13B, VPS28 +474 more	Copy number gain	not provided	GPathogenic
Select item 687018	GRCh37/hg19 8q21.13-21.2(chr8:83541047-86097857)x3	E2F5, LRRCC1 +1 more	Copy number gain	not provided	GUncertain significance
Select item 686594	GRCh37/hg19 8q21.2(chr8:86114785-86214050)x1	CA13, E2F5 +1 more	Copy number loss	not provided	GUncertain significance
Select item 685054	GRCh37/hg19 8q21.13-21.3(chr8:84358585-89159915)x1	ATP6V0D2, CA1 +16 more	Copy number loss	not provided	GUncertain significance
Select item 443619	GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	KCNQ3, KCNS2 +593 more	Copy number gain	See cases	GPathogenic
Select item 442201	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	PPDPFL, PPP1R16A +665 more	Copy number gain	See cases	GPathogenic
Select item 442200	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	AARD, ABRA +665 more	Copy number gain	See cases	GPathogenic
Select item 394884	GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	CLDN23, LONRF1 +665 more	Copy number gain	See cases	GPathogenic
Select item 155179	GRCh38/hg38 8q21.2-21.3(chr8:83721453-87866414)x3	ATP6V0D2, CA1 +46 more	Copy number gain	See cases	GUncertain significance
Select item 154791	GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	LOC129999937, LOC129999938 +3658 more	Copy number gain	See cases	GPathogenic
Select item 154530	GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3	LOC130001139, LOC130001140 +1686 more	Copy number gain	See cases	GPathogenic
Select item 153737	GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	LOC130000156, LOC130000157 +3106 more	Copy number gain	See cases	GPathogenic
Select item 153413	GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	AARD, ABRA +3658 more	Copy number gain	See cases	GPathogenic
Select item 150723	GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	LINC02894, LINC02906 +1960 more	Copy number gain	See cases	GPathogenic
Select item 150141	GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3	LOC130001211, LOC130001212 +1690 more	Copy number gain	See cases	GPathogenic
Select item 149660	GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	MIR7705, MIR7848 +3656 more	Copy number gain	See cases	GPathogenic
Select item 147946	GRCh38/hg38 8q13.1-22.1(chr8:66171669-93505509)x3	LOC130000602, LOC130000603 +470 more	Copy number gain	See cases	GPathogenic
Select item 147729	GRCh38/hg38 8q21.2(chr8:84246857-85606287)x1	CA1, CA13 +25 more	Copy number loss	See cases	GUncertain significance
Select item 60380	GRCh38/hg38 8q21.13-22.1(chr8:78672463-95366868)x1	LOC130000705, LOC130000706 +327 more	Copy number loss	See cases	GPathogenic
Select item 60379	GRCh38/hg38 8q21.13-21.3(chr8:77765431-91839285)x1	ATP6V0D2, C8orf88 +217 more	Copy number loss	See cases	GPathogenic
Select item 60377	GRCh38/hg38 8q21.11-21.2(chr8:73879385-85611466)x1	LOC130000617, LOC130000618 +191 more	Copy number loss	See cases	GPathogenic
Select item 59738	GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	PKHD1L1, PKIA +3656 more	Copy number gain	See cases	GPathogenic
Select item 57496	GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	LOC126860501, LOC126860502 +3652 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

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Germline classification

Types of conflicts

Molecular consequence

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Variation size

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Links from Gene

Items: 58