"GeneDx"[submitter] AND "RGS6"[gene] - ClinVar

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Search results

Items: 86

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58330	GRCh38/hg38 14q24.2(chr14:71647101-72567300)x3	LOC125048437, LOC126861990 +14 more	Copy number gain	See cases	GUncertain significance
Select item 152755	GRCh38/hg38 14q24.2(chr14:71864981-71952855)x3	LOC130056025, LOC130056026 +2 more	Copy number gain	See cases	GUncertain significance
Select item 1318175	NM_001204424.2(RGS6):c.-20-279C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1244827	NM_001204424.2(RGS6):c.-20-34C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182809	NM_001204424.2(RGS6):c.-20-25A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 145029	GRCh38/hg38 14q24.2(chr14:72172189-72198910)x3	RGS6	Copy number gain	See cases	GBenign
Select item 1317574	NM_001204424.2(RGS6):c.85-188G>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 783692	NM_001204424.2(RGS6):c.93C>T (p.Asp31=)	RGS6	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign/Likely benign
Select item 707930	NM_001204424.2(RGS6):c.184+7C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1317275	NM_001204424.2(RGS6):c.184+66C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1237670	NM_001204424.2(RGS6):c.235+131C>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316602	NM_001204424.2(RGS6):c.236-290A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317686	NM_001204424.2(RGS6):c.236-264C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316876	NM_001204424.2(RGS6):c.236-214T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1287731	NM_001204424.2(RGS6):c.342+86G>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261478	NM_001204424.2(RGS6):c.343-254T>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233646	NM_001204424.2(RGS6):c.343-199C>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235076	NM_001204424.2(RGS6):c.343-175A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1325932	NM_001204424.2(RGS6):c.343-96G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1706811	NM_001204424.2(RGS6):c.394+108G>C	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317456	NM_001204424.2(RGS6):c.395-207TGGA[14]	RGS6	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1287586	NM_001204424.2(RGS6):c.395-207TGGA[13]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1250892	NM_001204424.2(RGS6):c.395-207TGGA[11]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1222224	NM_001204424.2(RGS6):c.395-207TGGA[8]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1281038	NM_001204424.2(RGS6):c.395-164A>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273015	NM_001204424.2(RGS6):c.395-160A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262344	NM_001204424.2(RGS6):c.395-156T>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250540	NM_001204424.2(RGS6):c.395-155TGGGTGGA[2]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1224806	NM_001204424.2(RGS6):c.395-150G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235414	NM_001204424.2(RGS6):c.395-136_395-133del	RGS6	Deletion (intron variant)	not provided	GBenign
Select item 1265155	NM_001204424.2(RGS6):c.395-135TGGA[10]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1262192	NM_001204424.2(RGS6):c.395-135TGGA[11]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1245655	NM_001204424.2(RGS6):c.395-135TGGA[12]	RGS6	Microsatellite (intron variant)	not provided	GBenign
Select item 1224248	NM_001204424.2(RGS6):c.395-77G>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 789816	NM_001204424.2(RGS6):c.444G>C (p.Leu148=)	RGS6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1278178	NM_001204424.2(RGS6):c.459+33G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230444	NM_001204424.2(RGS6):c.459+279A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316464	NM_001204424.2(RGS6):c.460-254T>G	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317791	NM_001204424.2(RGS6):c.536+17G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1707294	NM_001204424.2(RGS6):c.536+147C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1286195	NM_001204424.2(RGS6):c.536+163T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243968	NM_001204424.2(RGS6):c.537-85C>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294533	NM_001204424.2(RGS6):c.618+74C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317922	NM_001204424.2(RGS6):c.618+261T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1282241	NM_001204424.2(RGS6):c.619-127_619-126insA	RGS6	Insertion (intron variant)	not provided	GBenign
Select item 1233517	NM_001204424.2(RGS6):c.619-126G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276978	NM_001204424.2(RGS6):c.694-274T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1329601	NM_001204424.2(RGS6):c.792+203C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1229193	NM_001204424.2(RGS6):c.792+204C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317017	NM_001204424.2(RGS6):c.793-283C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1224560	NM_001204424.2(RGS6):c.793-33T>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 677237	NM_001204424.2(RGS6):c.829T>C (p.Leu277=)	RGS6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1289871	NM_001204424.2(RGS6):c.855-262T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317801	NM_001204424.2(RGS6):c.965+185G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1180178	NM_001204424.2(RGS6):c.966-277T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242535	NM_001204424.2(RGS6):c.966-247T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290528	NM_001204424.2(RGS6):c.966-232G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317637	NM_001204424.2(RGS6):c.966-63G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1691596	NM_001204424.2(RGS6):c.1091+69TC[8]	RGS6	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1283136	NM_001204424.2(RGS6):c.1091+68_1091+69del	RGS6	Deletion (intron variant)	not provided	GBenign
Select item 1239824	NM_001204424.2(RGS6):c.1091+70C>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224100	NM_001204424.2(RGS6):c.1091+94A>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236481	NM_001204424.2(RGS6):c.1091+97A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247133	NM_001204424.2(RGS6):c.1091+167C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238943	NM_001204424.2(RGS6):c.1091+202G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272948	NM_001204424.2(RGS6):c.1091+212G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273550	NM_001204424.2(RGS6):c.1092-180A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 681492	NM_001204424.2(RGS6):c.1272C>T (p.Asp424=)	RGS6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1278645	NM_001204424.2(RGS6):c.1278+151C>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1331154	NM_001204424.2(RGS6):c.1368+20G>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1230879	NM_001204424.2(RGS6):c.1368+132G>T	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317206	NM_001204424.2(RGS6):c.1368+171C>G	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1288574	NM_001204424.2(RGS6):c.1368+197G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317205	NM_001204424.2(RGS6):c.1369-274G>A	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1235227	NM_001204424.2(RGS6):c.1369-251G>C	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182604	NM_001204424.2(RGS6):c.1369-170A>G	RGS6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317085	NM_001204424.2(RGS6):c.1422+77del	RGS6	Deletion (intron variant)	not provided	GLikely benign
Select item 1317738	NM_001204424.2(RGS6):c.1422+77T>C	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 151236	GRCh38/hg38 14q24.2(chr14:72557579-72709419)x3	DPF3, LOC126861992 +3 more	Copy number gain	See cases	GUncertain significance
Select item 1316742	NM_001204424.2(RGS6):c.1423-128G>T	RGS6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1258962	NM_001204424.2(RGS6):c.*3G>A	RGS6 (V445I +5 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not provided	GBenign
Select item 1317084	NM_001204424.2(RGS6):c.*113G>A	RGS6	Single nucleotide variant (3 prime UTR variant +3 more)	not provided	GLikely benign
Select item 1317911	NM_001204424.2(RGS6):c.*193G>T	RGS6	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1243582	NM_001204424.2(RGS6):c.*434C>T	RGS6	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GBenign
Select item 1316908	NM_001204424.2(RGS6):c.*469C>G	RGS6 (T627R)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1291958	NM_001204424.2(RGS6):c.*532T>C	RGS6 (L648P)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GBenign

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Items: 86