ClinVar for Gene (Select 222611) - ClinVar

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Links from Gene

Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3338185	NC_000006.12:g.47679135G>A	ADGRF2	Single nucleotide variant	Autism	GUncertain significance
Select item 3271327	NR_184444.1(ADGRF2):n.1971G>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3271317	NR_184444.1(ADGRF2):n.713T>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3271308	NR_184444.1(ADGRF2):n.2248T>G	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3271297	NR_184444.1(ADGRF2):n.831T>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085409	NR_184444.1(ADGRF2):n.1023T>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085392	NR_184444.1(ADGRF2):n.782A>G	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085367	NR_184444.1(ADGRF2):n.582T>A	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085325	NR_184444.1(ADGRF2):n.2103T>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085294	NR_184444.1(ADGRF2):n.1959G>A	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085227	NR_184444.1(ADGRF2):n.1548G>T	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3067227	NR_184444.1(ADGRF2):n.2032C>T	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 2623136	NR_184444.1(ADGRF2):n.1937G>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2618529	NR_184444.1(ADGRF2):n.1824A>G	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2557514	NR_184444.1(ADGRF2):n.2044C>G	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2546737	NR_184444.1(ADGRF2):n.2153C>G	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2528580	NR_184444.1(ADGRF2):n.852T>A	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2524201	NR_184444.1(ADGRF2):n.2254C>G	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2520844	NR_184444.1(ADGRF2):n.2193C>T	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2481070	NR_184444.1(ADGRF2):n.1091A>C	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2465158	NR_184444.1(ADGRF2):n.1755C>T	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2463004	NR_184444.1(ADGRF2):n.872G>A	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2462840	NR_184444.1(ADGRF2):n.2181G>T	ADGRF2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2377480	NC_000006.12:g.47680162A>G	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2374966	NC_000006.12:g.47682325T>G	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2374601	NC_000006.12:g.47681844T>C	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2367462	NC_000006.12:g.47681563C>T	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2353992	NC_000006.12:g.47682291A>T	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2344467	NC_000006.12:g.47682294G>C	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2338319	NC_000006.12:g.47682298C>A	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2311140	NC_000006.12:g.47682604T>G	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2302817	NC_000006.12:g.47681748T>C	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2254340	NC_000006.12:g.47682324C>A	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2251528	NC_000006.12:g.47682467T>G	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2249876	NC_000006.12:g.47679070G>T	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2244568	NC_000006.12:g.47682357A>G	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2240549	NC_000006.12:g.47681273C>A	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2236870	NC_000006.12:g.47682065C>A	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2226591	NC_000006.12:g.47680257A>C	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2219511	NC_000006.12:g.47681418G>C	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 2212751	NC_000006.12:g.47679055T>C	ADGRF2	Single nucleotide variant	not specified	GUncertain significance
Select item 1676306	GRCh37/hg19 6p21.1-q12(chr6:43636308-64947206)x3	PAQR8, PGK2 +92 more	Copy number gain	not provided	GLikely pathogenic
Select item 1527236	GRCh37/hg19 6p21.1-12.3(chr6:43636308-50947320)	ADGRF5, ANKRD66 +50 more	Copy number loss	not specified	GPathogenic
Select item 1341308	GRCh37/hg19 6p12.3(chr6:47410548-47701681)x3	ADGRF2, ADGRF4 +1 more	Copy number gain	not provided	GUncertain significance
Select item 625706	GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367)	ERVH-3, ETV7 +427 more	Copy number gain	not provided	GPathogenic
Select item 443497	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	AARS2, ABCC10 +1028 more	Copy number gain	See cases	GPathogenic
Select item 443496	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	RING1, RIOK1 +1028 more	Copy number gain	See cases	GPathogenic
Select item 153225	GRCh38/hg38 6p12.3(chr6:47191779-51427306)x1	ADGRF2, ADGRF4 +64 more	Copy number loss	See cases	GLikely pathogenic
Select item 149301	GRCh38/hg38 6p21.1-12.1(chr6:45681671-54212044)x1	GSTA3, GSTA4 +228 more	Copy number loss	See cases	GPathogenic
Select item 146275	GRCh38/hg38 6p21.1-12.3(chr6:44985760-47986838)x3	ADGRF1, ADGRF2 +78 more	Copy number gain	See cases	GLikely pathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

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Additional filters

Links from Gene

Items: 50