"GeneDx"[submitter] AND "WNT7A"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57977	GRCh38/hg38 3p26.3-24.3(chr3:63843-19510600)x3	LOC110120630, LOC111429626 +608 more	Copy number gain	See cases	GPathogenic
Select item 1212528	NM_004625.4(WNT7A):c.*132C>T	WNT7A	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 2348102	NM_004625.4(WNT7A):c.919A>T (p.Met307Leu)	WNT7A (M307L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 743183	NM_004625.4(WNT7A):c.624G>A (p.Ser208=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 35537	NM_004625.4(WNT7A):c.610G>A (p.Gly204Ser)	WNT7A (G204S)	Single nucleotide variant (missense variant)	Schinzel phocomelia syndrome +1 more	GPathogenic/Likely pathogenic
Select item 1222875	NM_004625.4(WNT7A):c.571-37T>C	WNT7A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283003	NM_004625.4(WNT7A):c.570+223A>G	LOC126806608, WNT7A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276828	NM_004625.4(WNT7A):c.570+212G>C	LOC126806608, WNT7A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1198399	NM_004625.4(WNT7A):c.570+79G>A	LOC126806608, WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1291668	NM_004625.4(WNT7A):c.459T>C (p.Ser153=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1278485	NM_004625.4(WNT7A):c.315G>A (p.Ala105=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1241552	NM_004625.4(WNT7A):c.298+203_298+210dup	WNT7A	Duplication (intron variant)	not provided	GBenign
Select item 1207079	NM_004625.4(WNT7A):c.298+40C>T	WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1286438	NM_004625.4(WNT7A):c.298+37C>A	WNT7A	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1212091	NM_004625.4(WNT7A):c.298+24C>T	WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 719319	NM_004625.4(WNT7A):c.81C>T (p.Ser27=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1240672	NM_004625.4(WNT7A):c.72-124C>A	WNT7A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254732	NM_004625.4(WNT7A):c.72-302G>A	WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1216573	NM_004625.4(WNT7A):c.71+230del	WNT7A	Deletion (intron variant)	not provided	GLikely benign
Select item 1218175	NM_004625.4(WNT7A):c.71+211G>C	WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1215877	NM_004625.4(WNT7A):c.71+100A>C	WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 787254	NM_004625.4(WNT7A):c.60C>T (p.Tyr20=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1203987	NM_004625.4(WNT7A):c.-123G>T	WNT7A	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1271514	NM_004625.4(WNT7A):c.-164C>A	WNT7A	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1204202	NM_004625.4(WNT7A):c.-168T>C	WNT7A	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1215167	NM_004625.4(WNT7A):c.-236G>A	WNT7A	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1200608	NC_000003.12:g.13880086G>C	WNT7A	Single nucleotide variant	not provided	GLikely benign
Select item 1280288	NC_000003.12:g.13880162G>T	WNT7A	Single nucleotide variant	not provided	GBenign
Select item 1190241	NC_000003.12:g.13880229C>G	WNT7A	Single nucleotide variant	not provided	GLikely benign
Select item 1328767	NC_000003.12:g.13880246G>T	WNT7A	Single nucleotide variant	not provided	GLikely benign
Select item 1207192	NC_000003.12:g.13880272C>T	WNT7A	Single nucleotide variant	not provided	GLikely benign
Select item 1231543	NC_000003.12:g.13880326C>T	WNT7A	Single nucleotide variant	not provided	GBenign
Select item 1706857	NC_000003.12:g.13880327C>T	WNT7A	Single nucleotide variant	not provided	GLikely benign

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Items: 33