ClinVar for Gene (Select 8013) - ClinVar

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Links from Gene

Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300978	NM_006981.4(NR4A3):c.1772G>A (p.Arg591Lys)	NR4A3 (R591K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300977	NM_006981.4(NR4A3):c.1515G>C (p.Gln505His)	NR4A3 (Q516H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300976	NM_006981.4(NR4A3):c.471C>G (p.Asp157Glu)	NR4A3 (D157E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300975	NM_006981.4(NR4A3):c.731G>T (p.Gly244Val)	NR4A3 (G255V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300974	NM_006981.4(NR4A3):c.398T>C (p.Met133Thr)	NR4A3 (M144T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201974	NM_006981.4(NR4A3):c.35C>T (p.Pro12Leu)	NR4A3 (P23L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201973	NM_006981.4(NR4A3):c.431C>G (p.Thr144Ser)	NR4A3 (T155S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201972	NM_006981.4(NR4A3):c.419C>T (p.Pro140Leu)	NR4A3 (P140L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201971	NM_006981.4(NR4A3):c.148A>G (p.Thr50Ala)	NR4A3 (T50A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201970	NM_006981.4(NR4A3):c.1547C>A (p.Ser516Tyr)	NR4A3 (S516Y +1 more)	Single nucleotide variant (missense variant)	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 3063058	GRCh37/hg19 9q31.1-31.2(chr9:102606857-109839724)x1	ABCA1, ALDOB +34 more	Copy number loss	not specified	GPathogenic
Select item 2671591	Single allele	CARD19, MIR24-1 +106 more	Deletion	not provided	GPathogenic
Select item 2590299	NM_006981.4(NR4A3):c.710C>A (p.Ala237Glu)	NR4A3 (A237E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544450	NM_006981.4(NR4A3):c.32C>T (p.Ser11Phe)	NR4A3 (S11F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543589	NM_006981.4(NR4A3):c.614C>G (p.Pro205Arg)	NR4A3 (P216R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542446	NM_006981.4(NR4A3):c.1682A>C (p.Lys561Thr)	NR4A3 (K572T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523706	NM_006981.4(NR4A3):c.666C>G (p.Ser222Arg)	NR4A3 (S222R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2499646	GRCh38/hg38 9q22.33-31.1(chr9:99779833-99839574)	LOC101928438, LOC126860703 +3 more	Copy number gain	Anomalous pulmonary venous return	GUncertain significance
Select item 2425182	NC_000009.11:g.(?_100190748)_(103062956_?)dup	ALG2, ANKS6 +22 more	Duplication	Congenital myasthenic syndrome 14 +2 more	GUncertain significance
Select item 2381811	NM_006981.4(NR4A3):c.1753G>C (p.Gly585Arg)	NR4A3 (G585R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2332192	NM_006981.4(NR4A3):c.1186A>G (p.Ile396Val)	LOC126860703, NR4A3 (I396V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2319421	NM_006981.4(NR4A3):c.1523G>A (p.Arg508His)	NR4A3 (R519H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318180	NM_006981.4(NR4A3):c.445C>T (p.Pro149Ser)	NR4A3 (P160S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281561	NM_006981.4(NR4A3):c.1088G>A (p.Arg363His)	LOC126860703, NR4A3 (R363H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259887	NM_006981.4(NR4A3):c.1156C>T (p.Pro386Ser)	LOC126860703, NR4A3 (P386S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1703688	GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311)	ATOSB, ATP6V1G1 +417 more	Copy number loss	Distal tetrasomy 15q	GUncertain significance
Select item 1527521	GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410)	ABCA1, ABHD17B +261 more	Copy number gain	not specified	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 1459792	NC_000009.11:g.(?_100190748)_(103062956_?)del	SEC61B, STX17 +22 more	Deletion	Nephronophthisis	GPathogenic
Select item 1341973	GRCh37/hg19 9q22.2-31.1(chr9:93864974-106661581)x1	ALDOB, ALG2 +87 more	Copy number loss	Gorlin syndrome	GPathogenic
Select item 997816	Single allele	PRXL2C, TBC1D2 +55 more	Deletion	Intellectual disability	GPathogenic
Select item 929316	GRCh37/hg19 9q22.31-31.2(chr9:96126075-108535272)x1	TSTD2, XPA +84 more	Copy number loss	See cases	GPathogenic
Select item 762601	NM_006981.4(NR4A3):c.1455-8C>A	NR4A3	Single nucleotide variant (intron variant)	not provided	GLikely benign
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 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 442793	GRCh37/hg19 9q22.32-31.1(chr9:97553176-102919383)x3	ALG2, ANKS6 +40 more	Copy number gain	See cases	GLikely pathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 161058	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	LOC126860732, LOC126860733 +514 more	Copy number loss	See cases	GPathogenic
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 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +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 151006	GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3	ABCA1, ABHD17B +1188 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 149230	GRCh38/hg38 9q22.33-31.3(chr9:99024205-109947890)x1	ABCA1, ABITRAM +253 more	Copy number loss	See cases	GPathogenic
Select item 147624	GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3	ABCA1, ABHD17B +1072 more	Copy number gain	See cases	GPathogenic
Select item 144971	GRCh38/hg38 9q22.32-31.3(chr9:95061030-108695569)x1	LOC130002205, LOC130002206 +417 more	Copy number loss	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 59881	GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3	LOC130002218, LOC130002219 +994 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 59123	GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1	CT70, CTNNAL1 +509 more	Copy number loss	See cases	GPathogenic
Select item 57370	GRCh38/hg38 9q22.33-31.1(chr9:99465640-100281736)x1	ERP44, INVS +21 more	Copy number loss	See cases	GUncertain significance
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 32222	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	ABCA1, ABITRAM +514 more	Copy number loss	See cases	GPathogenic

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Links from Gene

Items: 60