DVL1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	A2ML1-AS2, A3GALT2 +2151 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 58242	GRCh38/hg38 1p36.33-36.23(chr1:629025-8537745)x1	LOC121967050, LOC121967051 +520 more	Copy number loss	See cases	GPathogenic
Select item 58244	GRCh38/hg38 1p36.33-36.31(chr1:629044-7008678)x1	LOC129929262, LOC129929263 +458 more	Copy number loss	See cases	GPathogenic
Select item 58243	GRCh38/hg38 1p36.33-36.32(chr1:629044-3346226)x1	LOC129929093, LOC129929110 +282 more	Copy number loss	See cases	GPathogenic
Select item 151451	GRCh38/hg38 1p36.33-36.32(chr1:778698-4898439)x1	ACAP3, ACTRT2 +336 more	Copy number loss	See cases	GPathogenic
Select item 58036	GRCh38/hg38 1p36.33-36.32(chr1:792758-5006311)x3	LINC01786, LINC02593 +338 more	Copy number gain	See cases	GPathogenic
Select item 1684638	Single allele	TMEM240, TMEM88B +181 more	Deletion	Chromosome 1p36 deletion syndrome	GPathogenic
Select item 152849	GRCh38/hg38 1p36.33-36.32(chr1:821713-4225085)x1	LOC129929191, LOC129929192 +325 more	Copy number loss	See cases	GPathogenic
Select item 152807	GRCh38/hg38 1p36.33-36.32(chr1:821713-5099990)x1	ACAP3, ACTRT2 +337 more	Copy number loss	See cases	GPathogenic
Select item 152695	GRCh38/hg38 1p36.33-36.32(chr1:821713-2976123)x1	ACAP3, AGRN +254 more	Copy number loss	See cases	GPathogenic
Select item 152675	GRCh38/hg38 1p36.33-36.32(chr1:821713-2636393)x1	LOC129929104, LOC129929105 +249 more	Copy number loss	See cases	GPathogenic
Select item 152050	GRCh38/hg38 1p36.33-36.31(chr1:821713-5480263)x1	VWA1, WRAP73 +341 more	Copy number loss	See cases	GPathogenic
Select item 151110	GRCh38/hg38 1p36.33-36.32(chr1:821713-2554047)x1	ACAP3, AGRN +243 more	Copy number loss	See cases	GPathogenic
Select item 150995	GRCh38/hg38 1p36.33-36.32(chr1:821713-3438208)x1	ACAP3, ACTRT2 +275 more	Copy number loss	See cases	GPathogenic
Select item 149968	GRCh38/hg38 1p36.33-36.31(chr1:821713-7000838)x1	CEP104, CFAP74 +449 more	Copy number loss	See cases	GPathogenic
Select item 149171	GRCh38/hg38 1p36.33-36.32(chr1:821713-3569891)x1	ACAP3, ACTRT2 +284 more	Copy number loss	See cases	GPathogenic
Select item 149107	GRCh38/hg38 1p36.33-36.32(chr1:821713-3928354)x3	LOC129929084, LOC129929085 +320 more	Copy number gain	See cases	GLikely pathogenic
Select item 148916	GRCh38/hg38 1p36.33-36.32(chr1:821713-5239643)x1	ACAP3, ACTRT2 +337 more	Copy number loss	See cases	GPathogenic
Select item 148829	GRCh38/hg38 1p36.33-36.32(chr1:821713-2463016)x4	ACAP3, AGRN +238 more	Copy number gain	See cases	GUncertain significance
Select item 148825	GRCh38/hg38 1p36.33-36.32(chr1:821713-2463016)x1	ACAP3, AGRN +238 more	Copy number loss	See cases	GPathogenic
Select item 58245	GRCh38/hg38 1p36.33-36.32(chr1:821713-4155674)x1	ACAP3, ACTRT2 +325 more	Copy number loss	See cases	GPathogenic
Select item 58037	GRCh38/hg38 1p36.33-36.32(chr1:826553-4719105)x3	ACAP3, ACTRT2 +332 more	Copy number gain	See cases	GPathogenic
Select item 160923	GRCh38/hg38 1p36.33-36.32(chr1:844347-2627474)x1	ACAP3, AGRN +244 more	Copy number loss	See cases	GPathogenic
Select item 154642	GRCh38/hg38 1p36.33-36.23(chr1:844347-7870545)x1	PUSL1, RER1 +470 more	Copy number loss	See cases	GPathogenic
Select item 147521	GRCh38/hg38 1p36.33-36.22(chr1:844347-12470133)x1	ACAP3, ACOT7 +806 more	Copy number loss	See cases	GPathogenic
Select item 147354	GRCh38/hg38 1p36.33-36.23(chr1:844347-8171914)x1	LOC129929192, LOC129929193 +490 more	Copy number loss	See cases	GPathogenic
Select item 144707	GRCh38/hg38 1p36.33-36.32(chr1:844347-4398122)x1	ACAP3, ACTRT2 +325 more	Copy number loss	See cases	GPathogenic
Select item 144461	GRCh38/hg38 1p36.33-36.31(chr1:844347-6916587)x1	ACAP3, ACOT7 +441 more	Copy number loss	See cases	GPathogenic
Select item 58292	GRCh38/hg38 1p36.33(chr1:844347-2131805)x1	ACAP3, AGRN +205 more	Copy number loss	See cases	GPathogenic
Select item 58289	GRCh38/hg38 1p36.33-36.32(chr1:844347-4665295)x1	ACAP3, ACTRT2 +329 more	Copy number loss	See cases	GPathogenic
Select item 57440	GRCh38/hg38 1p36.33-36.31(chr1:844347-6477436)x1	ACAP3, ACOT7 +401 more	Copy number loss	See cases	GPathogenic
Select item 57218	GRCh38/hg38 1p36.33-36.32(chr1:844347-3712147)x1	ACAP3, ACTRT2 +292 more	Copy number loss	See cases	GPathogenic
Select item 57201	GRCh38/hg38 1p36.33-36.32(chr1:844347-3006252)x1	LOC129929161, LOC129929162 +252 more	Copy number loss	See cases	GPathogenic
Select item 57120	GRCh38/hg38 1p36.33-36.32(chr1:844347-2627474)x1	LOC129929114, LOC129929115 +244 more	Copy number loss	See cases	GPathogenic
Select item 57052	GRCh38/hg38 1p36.33-36.32(chr1:844347-3319395)x1	ACAP3, ACTRT2 +270 more	Copy number loss	See cases	GPathogenic
Select item 57049	GRCh38/hg38 1p36.33-36.31(chr1:844347-5682587)x1	LINC01786, LINC02593 +339 more	Copy number loss	See cases	GPathogenic
Select item 150566	GRCh38/hg38 1p36.33-36.31(chr1:844353-6477474)x1	LOC129929237, LOC129929238 +401 more	Copy number loss	See cases	GPathogenic
Select item 149739	GRCh38/hg38 1p36.33-36.32(chr1:844353-3153909)x1	ACAP3, ACTRT2 +260 more	Copy number loss	See cases	GPathogenic
Select item 145360	GRCh38/hg38 1p36.33-36.31(chr1:844353-5827192)x3	ACAP3, ACTRT2 +341 more	Copy number gain	See cases	GPathogenic
Select item 145356	GRCh38/hg38 1p36.33-36.32(chr1:844353-3487877)x1	ACAP3, ACTRT2 +274 more	Copy number loss	See cases	GPathogenic
Select item 144576	GRCh38/hg38 1p36.33-36.32(chr1:844353-2420916)x1	ACAP3, AGRN +234 more	Copy number loss	See cases	GPathogenic
Select item 58293	GRCh38/hg38 1p36.33-36.32(chr1:845437-2523513)x1	ACAP3, AGRN +237 more	Copy number loss	See cases	GPathogenic
Select item 58294	GRCh38/hg38 1p36.33-36.23(chr1:859215-8747647)x1	ACAP3, ACOT7 +519 more	Copy number loss	See cases	GPathogenic
Select item 58311	GRCh38/hg38 1p36.33-36.32(chr1:870177-4426613)x1	ACAP3, ACTRT2 +325 more	Copy number loss	See cases	GPathogenic
Select item 58316	GRCh38/hg38 1p36.33-36.32(chr1:872305-2642603)x1	ACAP3, AGRN +246 more	Copy number loss	See cases	GPathogenic
Select item 58315	GRCh38/hg38 1p36.33-36.32(chr1:872305-2642603)x3	ACAP3, AGRN +246 more	Copy number gain	See cases	GPathogenic
Select item 58314	GRCh38/hg38 1p36.33-36.32(chr1:872305-4133409)x1	ACAP3, ACTRT2 +320 more	Copy number loss	See cases	GPathogenic
Select item 58313	GRCh38/hg38 1p36.33-36.32(chr1:872305-3054463)x1	LOC126805582, LOC129388419 +253 more	Copy number loss	See cases	GPathogenic
Select item 58312	GRCh38/hg38 1p36.33(chr1:872305-2047715)x1	ACAP3, AGRN +198 more	Copy number loss	See cases	GPathogenic
Select item 147545	GRCh38/hg38 1p36.33-36.32(chr1:874379-4973261)x1	ACAP3, ACTRT2 +328 more	Copy number loss	See cases	GPathogenic
Select item 154584	GRCh38/hg38 1p36.33-36.23(chr1:898721-7811306)x1	LOC129929075, LOC129929076 +464 more	Copy number loss	See cases	GPathogenic
Select item 153078	GRCh38/hg38 1p36.33-36.22(chr1:902111-9556305)x1	ACAP3, ACOT7 +578 more	Copy number loss	See cases	GPathogenic
Select item 154687	GRCh38/hg38 1p36.33-36.32(chr1:911300-2963389)x1	ACAP3, AGRN +247 more	Copy number loss	See cases	GPathogenic
Select item 154548	GRCh38/hg38 1p36.33-36.22(chr1:911300-9329925)x1	LRRC47, MEGF6 +564 more	Copy number loss	See cases	GPathogenic
Select item 144176	GRCh38/hg38 1p36.33-36.32(chr1:911300-3614487)x3	ACAP3, ACTRT2 +277 more	Copy number gain	See cases	GPathogenic
Select item 155157	GRCh38/hg38 1p36.33(chr1:914086-1613769)x1	ACAP3, AGRN +146 more	Copy number loss	See cases	GPathogenic
Select item 154003	GRCh38/hg38 1p36.33(chr1:914086-1538895)x1	ACAP3, AGRN +136 more	Copy number loss	See cases	GLikely pathogenic
Select item 153663	GRCh38/hg38 1p36.33-36.22(chr1:914086-9567122)x1	LOC129929302, LOC129929303 +577 more	Copy number loss	See cases	GPathogenic
Select item 153195	GRCh38/hg38 1p36.33-36.32(chr1:914086-3587042)x1	ACAP3, ACTRT2 +277 more	Copy number loss	See cases	GPathogenic
Select item 152333	GRCh38/hg38 1p36.33-36.32(chr1:914086-3305463)x1	ACAP3, ACTRT2 +264 more	Copy number loss	See cases	GPathogenic
Select item 152331	GRCh38/hg38 1p36.33-36.32(chr1:914086-2465738)x1	LOC129929169, LOC129929170 +231 more	Copy number loss	See cases	GPathogenic
Select item 145604	GRCh38/hg38 1p36.33(chr1:932163-1792271)x4	ACAP3, AGRN +168 more	Copy number gain	See cases	GLikely benign
Select item 144721	GRCh38/hg38 1p36.33(chr1:1013081-1722599)x1	ACAP3, AGRN +137 more	Copy number loss	See cases	GPathogenic
Select item 148305	GRCh38/hg38 1p36.33-36.32(chr1:1022094-4665295)x1	ACAP3, ACTRT2 +301 more	Copy number loss	See cases	GPathogenic
Select item 149947	GRCh38/hg38 1p36.33-36.32(chr1:1072906-2806838)x1	ACAP3, ANKRD65 +209 more	Copy number loss	See cases	GPathogenic
Select item 144807	GRCh38/hg38 1p36.33-36.32(chr1:1118636-4179080)x1	ACAP3, ACTRT2 +273 more	Copy number loss	See cases	GPathogenic
Select item 58318	GRCh38/hg38 1p36.33-36.31(chr1:1181847-5507243)x1	ACAP3, ACTRT2 +273 more	Copy number loss	See cases	GPathogenic
Select item 150863	GRCh38/hg38 1p36.33-36.32(chr1:1330915-3743546)x3	LOC129929178, LOC129929179 +195 more	Copy number gain	See cases	GUncertain significance
Select item 3033799	NM_001330311.2(DVL1):c.*9G>A	DVL1	Single nucleotide variant (3 prime UTR variant)	DVL1-related disorder	GLikely benign
Select item 931592	NM_001330311.2(DVL1):c.2078_*7del (p.Asp693_Ter696delinsXaa)	DVL1	Deletion (stop lost)	Autosomal dominant Robinow syndrome 1	GUncertain significance
Select item 3005520	NM_001330311.2(DVL1):c.2084T>C (p.Met695Thr)	DVL1 (M695T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2887280	NM_001330311.2(DVL1):c.2074G>A (p.Val692Met)	DVL1 (V667M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2074381	NM_001330311.2(DVL1):c.2073C>T (p.Phe691=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2968422	NM_001330311.2(DVL1):c.2070C>A (p.Phe690Leu)	DVL1 (F665L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2575783	NM_001330311.2(DVL1):c.2069T>A (p.Phe690Tyr)	DVL1 (F665Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2703390	NM_001330311.2(DVL1):c.2066A>T (p.Glu689Val)	DVL1 (E689V +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2079190	NM_001330311.2(DVL1):c.2064C>T (p.Cys688=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 710582	NM_001330311.2(DVL1):c.2061C>T (p.Pro687=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1327733	NM_001330311.2(DVL1):c.2060C>G (p.Pro687Arg)	DVL1 (P662R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2955922	NM_001330311.2(DVL1):c.2059C>A (p.Pro687Thr)	DVL1 (P687T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808509	NM_001330311.2(DVL1):c.2051T>C (p.Met684Thr)	DVL1 (M659T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2553670	NM_001330311.2(DVL1):c.2050A>G (p.Met684Val)	DVL1 (M659V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1985396	NM_001330311.2(DVL1):c.2047G>A (p.Ala683Thr)	DVL1 (A683T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 737733	NM_001330311.2(DVL1):c.2043G>A (p.Gln681=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965735	NM_001330311.2(DVL1):c.2034G>T (p.Gln678His)	DVL1 (Q653H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1054652	NM_001330311.2(DVL1):c.2030G>A (p.Arg677His)	DVL1 (R652H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1357912	NM_001330311.2(DVL1):c.2029C>T (p.Arg677Cys)	DVL1 (R652C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1998197	NM_001330311.2(DVL1):c.2018T>C (p.Leu673Ser)	DVL1 (L648S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2280236	NM_001330311.2(DVL1):c.2015A>C (p.Glu672Ala)	DVL1 (E647A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1518905	NM_001330311.2(DVL1):c.2013G>A (p.Pro671=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1403373	NM_001330311.2(DVL1):c.2012C>T (p.Pro671Leu)	DVL1 (P646L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2980972	NM_001330311.2(DVL1):c.2007C>T (p.Val669=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1629973	NM_001330311.2(DVL1):c.2007C>G (p.Val669=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1562503	NM_001330311.2(DVL1):c.2005G>T (p.Val669Phe)	DVL1 (V644F +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant Robinow syndrome 2 +1 more	GConflicting classifications of pathogenicity
Select item 1224346	NM_001330311.2(DVL1):c.2005G>A (p.Val669Ile)	DVL1 (V644I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1077713	NM_001330311.2(DVL1):c.2004C>T (p.Ala668=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3001953	NM_001330311.2(DVL1):c.2000C>A (p.Ala667Asp)	DVL1 (A667D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1568528	NM_001330311.2(DVL1):c.1992G>A (p.Arg664=)	DVL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1056087	NM_001330311.2(DVL1):c.1991G>A (p.Arg664Gln)	DVL1 (R639Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2742244	NM_001330311.2(DVL1):c.1990C>T (p.Arg664Trp)	DVL1 (R664W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

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