14859[HGNC] - ClinVar

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Items: 54

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 145579	GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3	ABCA2, ABL1 +1272 more	Copy number gain	See cases	GPathogenic
Select item 57324	GRCh38/hg38 9q33.2-34.3(chr9:121112395-138075224)x3	ABCA2, ABL1 +1268 more	Copy number gain	See cases	GPathogenic
Select item 57353	GRCh38/hg38 9q33.2-34.3(chr9:122792658-138124532)x3	LOC130003132, LOC130003133 +1210 more	Copy number gain	See cases	GPathogenic
Select item 145575	GRCh38/hg38 9q34.11-34.3(chr9:129068560-138179445)x3	MED27, MIGA2 +789 more	Copy number gain	See cases	GPathogenic
Select item 59908	GRCh38/hg38 9q34.11-34.3(chr9:129068560-136495351)x3	ABL1, ABO +536 more	Copy number gain	See cases	GPathogenic
Select item 59135	GRCh38/hg38 9q34.11-34.13(chr9:129949815-132342490)x1	LOC130002822, LOC130002823 +160 more	Copy number loss	See cases	GPathogenic
Select item 144296	GRCh38/hg38 9q34.11-34.3(chr9:130513207-138124532)x3	LOC130003057, LOC130003058 +656 more	Copy number gain	See cases	GPathogenic
Select item 59909	GRCh38/hg38 9q34.13(chr9:131261516-131741175)x3	RAPGEF1, SNORD62A +57 more	Copy number gain	See cases	GPathogenic
Select item 2620672	NM_031432.5(UCK1):c.809T>C (p.Leu270Ser)	UCK1 (L247S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3185945	NM_031432.5(UCK1):c.749G>A (p.Arg250Gln)	UCK1 (R241Q +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2237996	NM_031432.5(UCK1):c.740G>T (p.Ser247Ile)	UCK1 (S252I +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3330767	NM_031432.5(UCK1):c.727T>C (p.Ser243Pro)	UCK1 (S234P +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2477802	NM_031432.5(UCK1):c.670G>A (p.Val224Met)	UCK1 (V201M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232404	NM_031432.5(UCK1):c.569T>C (p.Phe190Ser)	LOC126860779, UCK1 (F167S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2524146	NM_031432.5(UCK1):c.395C>T (p.Ala132Val)	LOC126860779, UCK1 (A132V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2458513	NM_031432.5(UCK1):c.380C>T (p.Thr127Met)	LOC126860779, UCK1 (T132M +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2392522	NM_031432.5(UCK1):c.373G>C (p.Glu125Gln)	LOC126860779, UCK1 (E116Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2253344	NM_031432.5(UCK1):c.312C>G (p.Ile104Met)	LOC126860779, UCK1 (I104M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330769	NM_031432.5(UCK1):c.218C>T (p.Ala73Val)	UCK1 (A73V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330770	NM_031432.5(UCK1):c.195C>G (p.Asp65Glu)	UCK1 (D56E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291548	NM_031432.5(UCK1):c.103G>A (p.Gly35Arg)	UCK1 (G35R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2513610	NM_031432.5(UCK1):c.59A>G (p.His20Arg)	UCK1 (H20R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185944	NM_031432.5(UCK1):c.14G>T (p.Gly5Val)	UCK1 (G5V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385279	NM_031432.5(UCK1):c.13G>A (p.Gly5Arg)	UCK1 (G5R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3245294	NC_000009.11:g.(?_131678355)_(140095163_?)dup	HMCN2, IER5L +147 more	Duplication	not provided	GUncertain significance
Select item 3245116	NC_000009.11:g.(?_131346980)_(135942612_?)dup	BARHL1, C9orf50 +62 more	Duplication	Early infantile epileptic encephalopathy with suppression bursts	GUncertain significance
Select item 3063111	GRCh37/hg19 9q34.13(chr9:134382079-134513578)x1	POMT1, RAPGEF1 +1 more	Copy number loss	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 2426262	NC_000009.11:g.(?_131087402)_(141016451_?)dup	ABCA2, ABL1 +187 more	Duplication	Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome	GUncertain significance
Select item 2425935	NC_000009.11:g.(?_131857676)_(135942612_?)dup	ABL1, AIF1L +45 more	Duplication	not provided	GUncertain significance
Select item 2425485	NC_000009.11:g.(?_133884602)_(135942612_?)dup	AIF1L, AK8 +21 more	Duplication	not provided	GUncertain significance
Select item 1804787	NC_000009.11:g.(134388719_134390812)_(134399194_?)del	POMT1, UCK1	Deletion	Autosomal recessive limb-girdle muscular dystrophy	GLikely pathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 815301	GRCh37/hg19 9q34.13(chr9:134035433-134400804)x3	FAM78A, PLPP7 +4 more	Copy number gain	not provided	GUncertain significance
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	AMBP, ANAPC2 +552 more	Copy number gain	not provided	GPathogenic
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 652388	NC_000009.11:g.(?_134379574)_(138678377_?)dup	ABO, ADAMTS13 +55 more	Duplication	Ehlers-Danlos syndrome, classic type	GUncertain significance
Select item 625553	GRCh37/hg19 9q34.11-34.13(chr9:131670024-134514071)	ABL1, AIF1L +38 more	Copy number loss	not provided	GLikely pathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ANGPTL2, ANKS6 +555 more	Copy number gain	Seizure +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	ODF2, OGN +769 more	Copy number gain	See cases	GPathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 395356	GRCh37/hg19 9q33.3-34.3(chr9:128652785-141044751)x3	ABCA2, ABL1 +228 more	Copy number gain	See cases	GPathogenic
Select item 394948	GRCh37/hg19 9q33.2-34.3(chr9:124642754-141146461)x3	ABCA2, ABL1 +279 more	Copy number gain	See cases	GPathogenic
Select item 253764	GRCh37/hg19 9q34.13(chr9:134353309-134839944)x3	POMT1, RAPGEF1 +3 more	Copy number gain	See cases	GUncertain significance
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic

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Items: 54