"GeneDx"[submitter] AND "FLI1"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59772	GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3	AASDHPPT, ABCG4 +1199 more	Copy number gain	See cases	GPathogenic
Select item 59777	GRCh38/hg38 11q23.3-25(chr11:120236432-135040246)x3	OR8G5, PANX3 +519 more	Copy number gain	See cases	GPathogenic
Select item 1241437	NM_001271012.2(FLI1):c.-203+7188del	FLI1, LOC128462394 +1 more	Deletion (intron variant)	not provided	GBenign
Select item 1284178	NM_001271012.2(FLI1):c.-203+7241GA[17]	FLI1, LOC128462394 +1 more	Microsatellite (intron variant)	not provided	GBenign
Select item 1280517	NM_001271012.2(FLI1):c.-203+7241GA[23]	FLI1, LOC128462394 +1 more	Microsatellite (intron variant)	not provided	GBenign
Select item 1276147	NM_001271012.2(FLI1):c.-203+7241GA[21]	FLI1, LOC128462394 +1 more	Microsatellite (intron variant)	not provided	GBenign
Select item 1235009	NM_001271012.2(FLI1):c.-203+7241GA[24]	FLI1, LOC128462394 +1 more	Microsatellite (intron variant)	not provided	GBenign
Select item 1232949	NM_001271012.2(FLI1):c.-203+7241GA[22]	SENCR, LOC128462394 +1 more	Microsatellite (intron variant)	not provided	GBenign
Select item 1307796	NM_002017.5(FLI1):c.16_18delinsT (p.Ile5_Lys6insTer)	FLI1, LOC128462394 +1 more	Indel (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 1253326	NM_002017.5(FLI1):c.18+205del	FLI1, SENCR	Deletion (intron variant)	not provided	GBenign
Select item 1283357	NM_002017.5(FLI1):c.18+226del	FLI1, SENCR	Deletion (intron variant)	not provided	GBenign
Select item 1288760	NM_002017.5(FLI1):c.18+239del	FLI1, SENCR	Deletion (intron variant)	not provided	GBenign
Select item 1282420	NM_002017.5(FLI1):c.18+247del	FLI1, SENCR	Deletion (intron variant)	not provided	GBenign
Select item 1244324	NM_002017.5(FLI1):c.18+270del	FLI1, SENCR	Deletion (intron variant)	not provided	GBenign
Select item 1252360	NM_002017.5(FLI1):c.18+306del	FLI1, SENCR	Deletion (intron variant)	not provided	GBenign
Select item 1233064	NM_002017.5(FLI1):c.18+311A>G	FLI1, SENCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227564	NM_002017.5(FLI1):c.18+316A>C	FLI1, SENCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246039	NM_002017.5(FLI1):c.19-284T>A	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1304260	NM_002017.5(FLI1):c.142A>T (p.Ile48Phe)	FLI1 (I15F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1274174	NM_002017.5(FLI1):c.230+202C>A	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243475	NM_002017.5(FLI1):c.230+202C>G	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234372	NM_002017.5(FLI1):c.230+249C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233290	NM_002017.5(FLI1):c.231-3788C>A	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295043	NM_002017.5(FLI1):c.231-3253C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246236	NM_002017.5(FLI1):c.231-305del	FLI1	Deletion (intron variant)	not provided	GBenign
Select item 1241777	NM_002017.5(FLI1):c.231-277G>A	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1240783	NM_002017.5(FLI1):c.231-214C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228311	NM_002017.5(FLI1):c.231-141A>G	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181710	NM_002017.5(FLI1):c.231-112C>A	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271621	NM_002017.5(FLI1):c.385+261A>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279874	NM_002017.5(FLI1):c.386-289C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261770	NM_002017.5(FLI1):c.589+99C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275393	NM_002017.5(FLI1):c.630A>G (p.Gln210=)	FLI1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1229941	NM_002017.5(FLI1):c.655+94G>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282188	NM_002017.5(FLI1):c.655+135_655+136insG	FLI1	Insertion (intron variant)	not provided	GBenign
Select item 1223172	NM_002017.5(FLI1):c.655+220T>G	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261919	NM_002017.5(FLI1):c.687T>A (p.Ala229=)	FLI1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1261722	NM_002017.5(FLI1):c.721+75C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182663	NM_002017.5(FLI1):c.722-207G>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282136	NM_002017.5(FLI1):c.722-162A>G	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288839	NM_002017.5(FLI1):c.722-95C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289892	NM_002017.5(FLI1):c.782-47A>G	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251150	NM_002017.5(FLI1):c.829+112G>C	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286405	NM_002017.5(FLI1):c.829+302G>A	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247227	NM_002017.5(FLI1):c.830-201C>T	FLI1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238677	NM_002017.5(FLI1):c.942C>G (p.Pro314=)	FLI1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 430313	NM_002017.5(FLI1):c.1019G>A (p.Arg340His)	FLI1 (R147H +3 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 424633	NM_002017.5(FLI1):c.1028A>G (p.Tyr343Cys)	FLI1 (Y343C +3 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2506873	NM_002017.5(FLI1):c.1134G>A (p.Met378Ile)	FLI1 (M185I +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 253601	GRCh37/hg19 11q23.3-25(chr11:119807473-134868407)x1	ACAD8, ACRV1 +113 more	Copy number loss	See cases	GPathogenic
Select item 253565	GRCh37/hg19 11q24.2-25(chr11:126631558-134868407)x1	NTM, NFRKB +32 more	Copy number loss	See cases	GPathogenic
Select item 253521	GRCh37/hg19 11q23.3-25(chr11:120615374-134868407)x1	CCDC15, CDON +108 more	Copy number loss	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 52