"GeneDx"[submitter] AND "GAS7"[gene] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1260702	NM_201433.2(GAS7):c.*267A>G	GAS7	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1222796	NM_201433.2(GAS7):c.1318-37G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273039	NM_201433.2(GAS7):c.1318-81T>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270921	NM_201433.2(GAS7):c.1318-95C>G	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295084	NM_201433.2(GAS7):c.1318-173G>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266608	NM_201433.2(GAS7):c.1318-225G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178248	NM_201433.2(GAS7):c.1317+195G>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271504	NM_201433.2(GAS7):c.1317+69G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286767	NM_201433.2(GAS7):c.1219-36G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228161	NM_201433.2(GAS7):c.1219-58G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182682	NM_201433.2(GAS7):c.1219-169A>G	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178676	NM_201433.2(GAS7):c.1219-201dup	GAS7	Duplication (intron variant)	not provided	GBenign
Select item 1220556	NM_201433.2(GAS7):c.1219-202A>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249262	NM_201433.2(GAS7):c.1218+185A>G	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1220653	NM_201433.2(GAS7):c.1138+282dup	GAS7	Duplication (intron variant)	not provided	GBenign
Select item 1288305	NM_201433.2(GAS7):c.1138+277G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226902	NM_201433.2(GAS7):c.1138+42_1138+44del	GAS7	Deletion (intron variant)	not provided	GBenign
Select item 1183597	NM_201433.2(GAS7):c.1015-340A>G	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183460	NM_201433.2(GAS7):c.1014+325G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279691	NM_201433.2(GAS7):c.1014+292C>G	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278147	NM_201433.2(GAS7):c.1014+277C>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228795	NM_201433.2(GAS7):c.1014+72C>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247390	NM_201433.2(GAS7):c.886-14T>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232749	NM_201433.2(GAS7):c.886-85G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1284057	NM_201433.2(GAS7):c.886-208G>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288958	NM_201433.2(GAS7):c.886-277del	GAS7	Deletion (intron variant)	not provided	GBenign
Select item 1228637	NM_201433.2(GAS7):c.806+227C>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268079	NM_201433.2(GAS7):c.731+226_731+239del	GAS7	Deletion (intron variant)	not provided	GBenign
Select item 1281885	NM_201433.2(GAS7):c.731+164A>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237981	NM_201433.2(GAS7):c.731+73C>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183433	NM_201433.2(GAS7):c.731+49C>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283238	NM_201433.2(GAS7):c.648C>G (p.Thr216=)	GAS7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1221563	NM_201433.2(GAS7):c.616-78C>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249025	NM_201433.2(GAS7):c.616-171G>T	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237121	NM_201433.2(GAS7):c.615+82T>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231024	NM_201433.2(GAS7):c.526-140G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232093	NM_201433.2(GAS7):c.526-179G>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279386	NM_201433.2(GAS7):c.472-427A>G	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1255118	NM_201433.2(GAS7):c.471+226T>C	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272907	NM_201433.2(GAS7):c.471+16G>A	GAS7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 60132	GRCh38/hg38 17p13.1(chr17:10084941-10502052)x3	GAS7, LOC112529894 +17 more	Copy number gain	See cases	GUncertain significance
Select item 60133	GRCh38/hg38 17p13.1(chr17:10112910-10477423)x3	GAS7, LOC112529894 +14 more	Copy number gain	See cases	GUncertain significance

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Items: 42