348793[Gene ID] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145614	GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	LOC115995524, LOC115995525 +2647 more	Copy number gain	See cases	GPathogenic
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	LOC123453201, LOC123453202 +1450 more	Copy number gain	See cases	GPathogenic
Select item 150609	GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	LOC129938169, LOC129938170 +1318 more	Copy number gain	See cases	GPathogenic
Select item 154213	GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3	LOC108281160, LOC108281177 +1247 more	Copy number gain	See cases	GPathogenic
Select item 152257	GRCh38/hg38 3q25.31-29(chr3:156321878-198113452)x3	ABCC5, ABCC5-AS1 +1245 more	Copy number gain	See cases	GPathogenic
Select item 57984	GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3	LOC132088897, LOC132088898 +1201 more	Copy number gain	See cases	GPathogenic
Select item 155627	GRCh38/hg38 3q26.1-29(chr3:166137209-198125115)x3	LOC129938260, LOC129938261 +1064 more	Copy number gain	See cases	GPathogenic
Select item 148012	GRCh38/hg38 3q26.2-29(chr3:168167568-198110178)x3	LOC129938077, LOC129938078 +1041 more	Copy number gain	See cases	GPathogenic
Select item 149685	GRCh38/hg38 3q26.32-29(chr3:176168525-198118383)x3	ZMAT3, ZNF639 +867 more	Copy number gain	See cases	GPathogenic
Select item 148947	GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3	LOC129938282, LOC129938283 +866 more	Copy number gain	See cases	GPathogenic
Select item 57868	GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1	MIR944, MUC20 +557 more	Copy number loss	See cases	GPathogenic
Select item 57997	GRCh38/hg38 3q28-29(chr3:189265371-198110178)x3	ACAP2, APOD +411 more	Copy number gain	See cases	GPathogenic
Select item 57998	GRCh38/hg38 3q28-29(chr3:190667663-198110178)x3	LOC126806930, LOC126806931 +375 more	Copy number gain	See cases	GPathogenic
Select item 148761	GRCh38/hg38 3q29(chr3:192752937-198118383)x3	ACAP2, APOD +337 more	Copy number gain	See cases	GPathogenic
Select item 155434	GRCh38/hg38 3q29(chr3:193704605-198125115)x3	TM4SF19-DYNLT2B, TMEM44 +313 more	Copy number gain	See cases	GPathogenic
Select item 149477	GRCh38/hg38 3q29(chr3:194296197-198110198)x3	ACAP2, APOD +273 more	Copy number gain	See cases	GPathogenic
Select item 147306	GRCh38/hg38 3q29(chr3:194338534-197693741)x1	ACAP2, APOD +239 more	Copy number loss	See cases	GPathogenic
Select item 58000	GRCh38/hg38 3q29(chr3:194424496-198168758)x3	RUBCN, SENP5 +264 more	Copy number gain	See cases	GPathogenic
Select item 148016	GRCh38/hg38 3q29(chr3:195711798-198110178)x3	BDH1, CEP19 +169 more	Copy number gain	See cases	GPathogenic
Select item 59685	GRCh38/hg38 3q29(chr3:195711798-197976152)x3	LOC129938284, LOC129938285 +166 more	Copy number gain	See cases	GUncertain significance
Select item 59981	GRCh38/hg38 3q29(chr3:195755702-197583580)x3	LOC129938303, LOC129938304 +133 more	Copy number gain	See cases	GPathogenic
Select item 1679598	Single allele	SENP5, SLC51A +114 more	Deletion	Chromosome 3q29 microdeletion syndrome	GPathogenic
Select item 59686	GRCh38/hg38 3q29(chr3:195896948-198110178)x3	BDH1, CEP19 +155 more	Copy number gain	See cases	GUncertain significance
Select item 545293	Single allele	LOC123464504, LOC129938307 +114 more	Duplication	Autism	GLikely pathogenic
Select item 2499658	GRCh38/hg38 3q29(chr3:195950438-197629463)	BDH1, CEP19 +113 more	Copy number loss	See cases	GPathogenic
Select item 149940	GRCh38/hg38 3q29(chr3:195955711-197597912)x1	BDH1, CEP19 +111 more	Copy number loss	See cases	GPathogenic
Select item 155422	GRCh38/hg38 3q29(chr3:195963356-197629463)x3	FBXO45, LINC00885 +110 more	Copy number gain	See cases	GUncertain significance
Select item 59982	GRCh38/hg38 3q29(chr3:195965316-197625573)x3	BDH1, CEP19 +109 more	Copy number gain	See cases	GPathogenic
Select item 59983	GRCh38/hg38 3q29(chr3:195972720-197658495)x3	BDH1, CEP19 +113 more	Copy number gain	See cases	GPathogenic
Select item 148628	GRCh38/hg38 3q29(chr3:195974291-197597912)x1	NRROS, PAK2 +109 more	Copy number loss	See cases	GPathogenic
Select item 153972	GRCh38/hg38 3q29(chr3:195976744-197629463)x1	BDH1, CEP19 +110 more	Copy number loss	See cases	GPathogenic
Select item 545294	NC_000003.12:g.(?_195990063)_(197617301_?)del	LOC123464504, LOC123464505 +108 more	Deletion	Schizophrenia	GPathogenic
Select item 59984	GRCh38/hg38 3q29(chr3:195997494-197662231)x3	BDH1, CEP19 +111 more	Copy number gain	See cases	GPathogenic
Select item 153314	GRCh38/hg38 3q29(chr3:195998419-197629463)x3	BDH1, CEP19 +108 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 160933	GRCh38/hg38 3q29(chr3:196013486-197590232)x3	BDH1, CEP19 +107 more	Copy number gain	See cases	GPathogenic
Select item 160885	GRCh38/hg38 3q29(chr3:196013486-197590232)x1	BDH1, CEP19 +107 more	Copy number loss	See cases	GPathogenic
Select item 154986	GRCh38/hg38 3q29(chr3:196013486-197597912)x1	BDH1, CEP19 +107 more	Copy number loss	See cases	GPathogenic
Select item 152467	GRCh38/hg38 3q29(chr3:196013486-197612399)x1	BDH1, CEP19 +107 more	Copy number loss	See cases	GPathogenic
Select item 57328	GRCh38/hg38 3q29(chr3:196013486-197503306)x3	CEP19, DLG1 +102 more	Copy number gain	See cases	GPathogenic
Select item 34369	GRCh38/hg38 3q29(chr3:196013486-197590232)x1	LOC129938306, LOC129938307 +107 more	Copy number loss	See cases	GPathogenic
Select item 149576	GRCh38/hg38 3q29(chr3:196013531-197590232)x1	BDH1, CEP19 +107 more	Copy number loss	See cases	GPathogenic
Select item 59986	GRCh38/hg38 3q29(chr3:196035777-197662231)x3	BDH1, CEP19 +111 more	Copy number gain	See cases	GPathogenic
Select item 59985	GRCh38/hg38 3q29(chr3:196035777-197606438)x3	BDH1, CEP19 +107 more	Copy number gain	See cases	GPathogenic
Select item 59289	GRCh38/hg38 3q29(chr3:196035777-197625573)x1	BDH1, CEP19 +107 more	Copy number loss	See cases	GPathogenic
Select item 59288	GRCh38/hg38 3q29(chr3:196035777-197658540)x1	BDH1, CEP19 +111 more	Copy number loss	See cases	GPathogenic
Select item 57492	GRCh38/hg38 3q29(chr3:196077857-197165715)x1	CEP19, DLG1 +89 more	Copy number loss	See cases	GPathogenic
Select item 545295	NC_000003.12:g.(?_196154147)_(197376501_?)del	CEP19, DLG1 +85 more	Deletion	Schizophrenia	GPathogenic
Select item 153416	GRCh38/hg38 3q29(chr3:196418334-198125115)x3	BDH1, CEP19 +102 more	Copy number gain	See cases	GUncertain significance
Select item 144313	GRCh38/hg38 3q29(chr3:196536193-196741662)x3	CEP19, FBXO45 +19 more	Copy number gain	See cases	GUncertain significance
Select item 2213514	NM_182627.3(WDR53):c.1048A>G (p.Ile350Val)	WDR53 (I191V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190100	NM_182627.3(WDR53):c.1042A>G (p.Ser348Gly)	WDR53 (S348G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190099	NM_182627.3(WDR53):c.1022T>C (p.Ile341Thr)	WDR53 (I180T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381579	NM_182627.3(WDR53):c.851G>A (p.Arg284His)	WDR53 (R125H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190107	NM_182627.3(WDR53):c.797C>T (p.Thr266Met)	WDR53 (T105M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2343935	NM_182627.3(WDR53):c.792G>T (p.Lys264Asn)	WDR53 (K105N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190106	NM_182627.3(WDR53):c.766C>A (p.Leu256Met)	WDR53 (L256M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314533	NM_182627.3(WDR53):c.689A>C (p.Lys230Thr)	WDR53 (K69T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492346	NM_182627.3(WDR53):c.674G>A (p.Arg225Gln)	WDR53 (R225Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525689	NM_182627.3(WDR53):c.665G>A (p.Arg222Gln)	WDR53 (R61Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190105	NM_182627.3(WDR53):c.592G>A (p.Ala198Thr)	WDR53 (A39T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539570	NM_182627.3(WDR53):c.589C>T (p.Pro197Ser)	WDR53 (P197S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332862	NM_182627.3(WDR53):c.508C>G (p.Arg170Gly)	WDR53 (R11G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190104	NM_182627.3(WDR53):c.449A>C (p.Gln150Pro)	WDR53 (Q150P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332861	NM_182627.3(WDR53):c.441G>C (p.Gln147His)	WDR53 (Q147H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513383	NM_182627.3(WDR53):c.410A>G (p.Asn137Ser)	WDR53 (N137S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190103	NM_182627.3(WDR53):c.368T>G (p.Leu123Trp)	WDR53 (L123W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267708	NM_182627.3(WDR53):c.229G>A (p.Val77Ile)	WDR53 (V77I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2204170	NM_182627.3(WDR53):c.220A>T (p.Thr74Ser)	WDR53 (T74S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332860	NM_182627.3(WDR53):c.122C>T (p.Thr41Ile)	WDR53 (T41I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354144	NM_182627.3(WDR53):c.101C>T (p.Thr34Met)	WDR53 (T34M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2231468	NM_182627.3(WDR53):c.74C>T (p.Ala25Val)	WDR53 (A25V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190102	NM_182627.3(WDR53):c.27T>G (p.His9Gln)	WDR53 (H9Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618225	NM_182627.3(WDR53):c.26A>G (p.His9Arg)	WDR53 (H9R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190101	NM_182627.3(WDR53):c.11A>G (p.Lys4Arg)	WDR53 (K4R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3242309	GRCh37/hg19 3q29(chr3:195106447-197846145)x3	ACAP2, APOD +33 more	Copy number gain	not provided	GPathogenic
Select item 3148910	GRCh37/hg19 3q26.33-29(chr3:179313373-197851444)x3	ABCC5, ABCF3 +136 more	Copy number gain	See cases	GPathogenic
Select item 3148878	GRCh37/hg19 3q29(chr3:195739427-197340833)x1	BDH1, CEP19 +19 more	Copy number loss	not provided	GPathogenic
Select item 2685951	GRCh37/hg19 3q29(chr3:196190723-197605588)x3	BDH1, CEP19 +15 more	Copy number gain	not provided	GPathogenic
Select item 2671619	Single allele	ABCC5, ABCF3 +145 more	Duplication	not provided	GPathogenic
Select item 2671595	Single allele	MUC20, MUC4 +286 more	Duplication	not provided	GPathogenic
Select item 2445506	NC_000003.11:g.(?_195591052)_(197682644_?)dup	BDH1, CEP19 +26 more	Duplication	not provided	GUncertain significance
Select item 1809243	GRCh37/hg19 3q29(chr3:195790857-196543483)x1	CEP19, DYNLT2B +13 more	Copy number loss	not provided	GUncertain significance
Select item 1808666	GRCh37/hg19 3q29(chr3:195690228-197356334)x1	BDH1, CEP19 +19 more	Copy number loss	not provided	GPathogenic
Select item 1707630	GRCh37/hg19 3q26.31-29(chr3:171558472-197871052)x3	CCDC50, MELTF +155 more	Copy number gain	Isolated anorectal malformation	GLikely pathogenic
Select item 1707428	GRCh37/hg19 3q27.1-29(chr3:183498520-197851986)x3	ABCC5, ABCF3 +118 more	Copy number gain	See cases	GPathogenic
Select item 1703655	GRCh37/hg19 3q29(chr3:195703615-197386180)	BDH1, CEP19 +19 more	Copy number loss	Chromosome 3q29 microdeletion syndrome	GPathogenic
Select item 1340723	GRCh37/hg19 3q29(chr3:195914129-196804639)x1	CEP19, DLG1 +17 more	Copy number loss	not provided	GPathogenic
Select item 1340518	GRCh37/hg19 3q29(chr3:195993691-197851986)x3	BDH1, CEP19 +22 more	Copy number gain	not provided	GUncertain significance
Select item 1340375	GRCh37/hg19 3q29(chr3:196269417-196481401)x3	CEP19, FBXO45 +4 more	Copy number gain	not provided	GLikely benign
Select item 1330171	GRCh37/hg19 3q29(chr3:194790394-197961930)x3	ACAP2, APOD +35 more	Copy number gain	Chromosome 3q29 microdeletion syndrome	GUncertain significance
Select item 1328450	GRCh37/hg19 3q28-29(chr3:191866466-197842171)x1	ACAP2, APOD +48 more	Copy number loss	not provided	GPathogenic
Select item 1326307	GRCh37/hg19 3q28-29(chr3:189608636-197532175)x1	OPA1, OSTN +56 more	Copy number loss	3q28q29 deletion syndrome	GPathogenic
Select item 1172568	GRCh37/hg19 3q29(chr3:195693872-197376871)x3	BDH1, CEP19 +19 more	Copy number gain	See cases	Grisk factor
Select item 1015396	NC_000003.11:g.(?_195754030)_(196438852_?)dup	CEP19, DYNLT2B +11 more	Duplication	not provided	GUncertain significance
Select item 997056	GRCh37/hg19 3q29(chr3:195419168-197387258)	UBXN7, BDH1 +24 more	Copy number gain	Delayed speech and language development +1 more	GPathogenic
Select item 997046	GRCh37/hg19 3q29(chr3:195747856-197387258)	SENP5, SLC51A +19 more	Copy number gain	Motor delay +1 more	GPathogenic
Select item 980655	GRCh37/hg19 3q29(chr3:195068028-197851986)x3	DLG1, PPP1R2 +33 more	Copy number gain	not provided	GPathogenic
Select item 816511	GRCh37/hg19 3q29(chr3:195652973-197346971)x1	BDH1, WDR53 +19 more	Copy number loss	See cases	GPathogenic
Select item 814513	GRCh37/hg19 3q29(chr3:196244688-196535851)x3	FBXO45, WDR53 +4 more	Copy number gain	not provided	GUncertain significance
Select item 814512	GRCh37/hg19 3q29(chr3:195848341-196426606)x3	UBXN7, ZDHHC19 +9 more	Copy number gain	not provided	GUncertain significance

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