"GeneDx"[submitter] AND "ELOVL5"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1343009	NM_021814.5(ELOVL5):c.*77A>G	ELOVL5	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 1316416	NM_021814.5(ELOVL5):c.861G>T (p.Leu287=)	ELOVL5 (G246*)	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 218139	NM_021814.5(ELOVL5):c.757-40_757-37dup	ELOVL5	Duplication (intron variant)	not provided	GBenign
Select item 1248305	NM_021814.5(ELOVL5):c.757-97_757-96insAAAAG	ELOVL5	Insertion (intron variant)	not provided	GBenign
Select item 1321663	NM_021814.5(ELOVL5):c.757-181dup	ELOVL5	Duplication (intron variant)	not provided	GLikely benign
Select item 1293375	NM_021814.5(ELOVL5):c.757-233T>C	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1344981	NM_021814.5(ELOVL5):c.622-12C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1282019	NM_021814.5(ELOVL5):c.621+299_621+308del	ELOVL5	Deletion (intron variant)	not provided	GBenign
Select item 1321626	NM_021814.5(ELOVL5):c.497-63_497-62del	ELOVL5	Deletion (intron variant)	not provided	GLikely benign
Select item 1221576	NM_021814.5(ELOVL5):c.497-62del	ELOVL5	Deletion (intron variant)	not provided	GBenign
Select item 1258670	NM_021814.5(ELOVL5):c.497-118C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1706184	NM_021814.5(ELOVL5):c.496+84T>G	ELOVL5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1269783	NM_021814.5(ELOVL5):c.325-102C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257447	NM_021814.5(ELOVL5):c.324+217C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289470	NM_021814.5(ELOVL5):c.324+49A>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1706227	NM_021814.5(ELOVL5):c.324+25TAT[4]	ELOVL5	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1707374	NM_021814.5(ELOVL5):c.324+32A>G	ELOVL5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1285668	NM_021814.5(ELOVL5):c.247-150T>G	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1321793	NM_021814.5(ELOVL5):c.246+4089C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1239255	NM_021814.5(ELOVL5):c.246+3932C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 691282	NM_021814.5(ELOVL5):c.246+3891C>T	ELOVL5 (Q102*)	Single nucleotide variant (nonsense +1 more)	not provided	GBenign/Likely benign
Select item 1707196	NM_021814.5(ELOVL5):c.246+3863C>G	ELOVL5	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 1293370	NM_021814.5(ELOVL5):c.246+3816T>C	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248389	NM_021814.5(ELOVL5):c.246+3729A>C	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249097	NM_021814.5(ELOVL5):c.246+110T>G	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1683802	NM_021814.5(ELOVL5):c.59-169C>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1180857	NM_021814.5(ELOVL5):c.58+1350C>A	ELOVL5	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1286265	NM_021814.5(ELOVL5):c.58+1207C>T	ELOVL5	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1258723	NM_021814.5(ELOVL5):c.58+1041A>G	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236544	NM_021814.5(ELOVL5):c.58+893G>A	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248645	NM_021814.5(ELOVL5):c.58+864A>G	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222905	NM_021814.5(ELOVL5):c.58+207A>T	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239418	NM_021814.5(ELOVL5):c.58+96G>A	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293074	NM_021814.5(ELOVL5):c.58+57C>A	ELOVL5	Single nucleotide variant (intron variant)	not provided	GBenign

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Items: 34