ClinVar for Gene (Select 165257) - ClinVar

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Links from Gene

Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3135725	NM_182528.4(C1QL2):c.679G>C (p.Gly227Arg)	C1QL2 (G227R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135724	NM_182528.4(C1QL2):c.374C>T (p.Thr125Met)	C1QL2 (T125M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135723	NM_182528.4(C1QL2):c.293C>T (p.Pro98Leu)	C1QL2 (P98L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062651	GRCh37/hg19 2q12.2-21.2(chr2:106755586-134302739)x1	ACOXL, ACTR3 +121 more	Copy number loss	not specified	GPathogenic
Select item 3062627	GRCh37/hg19 2q14.1-14.3(chr2:116646793-126388760)x1	C1QL2, C2orf76 +22 more	Copy number loss	not specified	GLikely pathogenic
Select item 2618535	NM_182528.4(C1QL2):c.755A>C (p.His252Pro)	C1QL2 (H252P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599173	NM_182528.4(C1QL2):c.257A>G (p.Lys86Arg)	C1QL2 (K86R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551483	NM_182528.4(C1QL2):c.198C>A (p.Ser66Arg)	C1QL2 (S66R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525614	NM_182528.4(C1QL2):c.251C>T (p.Pro84Leu)	C1QL2 (P84L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475559	NM_182528.4(C1QL2):c.29C>T (p.Pro10Leu)	C1QL2 (P10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454403	NM_182528.4(C1QL2):c.412G>A (p.Val138Ile)	C1QL2 (V138I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403863	NM_182528.4(C1QL2):c.100G>T (p.Asp34Tyr)	C1QL2 (D34Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309126	NM_182528.4(C1QL2):c.376G>A (p.Ala126Thr)	C1QL2 (A126T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304900	NM_182528.4(C1QL2):c.238G>T (p.Asp80Tyr)	C1QL2 (D80Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273630	NM_182528.4(C1QL2):c.127G>A (p.Glu43Lys)	C1QL2 (E43K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251428	NM_182528.4(C1QL2):c.383G>A (p.Gly128Asp)	C1QL2 (G128D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247665	NM_182528.4(C1QL2):c.568C>A (p.Pro190Thr)	C1QL2 (P190T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210043	NM_182528.4(C1QL2):c.205C>T (p.Pro69Ser)	C1QL2 (P69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809385	GRCh37/hg19 2q14.1-14.3(chr2:116761476-123897262)x1	C1QL2, C2orf76 +21 more	Copy number loss	not provided	GPathogenic
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1679114	GRCh37/hg19 2q13-22.3(chr2:112475655-145691999)x3	EPB41L5, ERCC3 +120 more	Copy number gain	2q13q22.3 microduplication syndrome	GPathogenic
Select item 1526888	GRCh37/hg19 2q13-14.3(chr2:113188197-128144700)	ACTR3, BIN1 +51 more	Copy number loss	not specified	GPathogenic
Select item 1341292	GRCh37/hg19 2q14.2(chr2:118991485-120025223)x1	C1QL2, EN1 +2 more	Copy number loss	not provided	GUncertain significance
Select item 1340017	GRCh37/hg19 2q13-22.3(chr2:111484468-146333604)x3	GPR39, IL1F10 +122 more	Copy number gain	not provided	GPathogenic
Select item 814300	GRCh37/hg19 2q14.2(chr2:119905466-120016024)x1	STEAP3, C1QL2	Copy number loss	not provided	GUncertain significance
Select item 814299	GRCh37/hg19 2q14.2(chr2:119859810-120157980)x3	DBI, C2orf76 +2 more	Copy number gain	not provided	GLikely benign
Select item 814298	GRCh37/hg19 2q14.2-14.3(chr2:118903294-123099547)x1	TMEM177, TFCP2L1 +18 more	Copy number loss	not provided	GPathogenic
Select item 814297	GRCh37/hg19 2q14.2-14.3(chr2:118872395-128069813)x1	BIN1, PTPN4 +24 more	Copy number loss	not provided	GPathogenic
Select item 814296	GRCh37/hg19 2q14.1-14.2(chr2:115416190-122399064)x1	TMEM177, C2orf76 +20 more	Copy number loss	not provided	GPathogenic
Select item 778000	NM_182528.4(C1QL2):c.96C>A (p.Ile32=)	C1QL2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 562675	GRCh37/hg19 2q14.1-14.3(chr2:114707932-124328692)x1	STEAP3, PTPN4 +23 more	Copy number loss	not provided	GPathogenic
Select item 524189	Single allele	ACMSD, C2orf27A +486 more	Deletion	not provided	GLikely pathogenic
Select item 523163	GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1	CCDC74B, CCDC93 +218 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	RGPD4, RGPD5 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	IL1F10, IL1R1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442443	GRCh37/hg19 2q14.1-14.3(chr2:116754600-123897370)x1	C1QL2, C2orf76 +21 more	Copy number loss	See cases	GPathogenic
Select item 442204	GRCh37/hg19 2q13-14.3(chr2:114056441-123673800)x1	FOXD4L1, ACTR3 +27 more	Copy number loss	See cases	GPathogenic
Select item 253388	GRCh37/hg19 2q12.3-14.3(chr2:109798247-125658380)x1	RGPD8, ACTR3 +63 more	Copy number loss	See cases	GPathogenic
Select item 155658	GRCh38/hg38 2q14.2-14.3(chr2:118687829-121621814)x1	C1QL2, C2orf76 +92 more	Copy number loss	See cases	GPathogenic
Select item 153085	GRCh38/hg38 2q14.1-14.3(chr2:115302067-129071130)x1	AMMECR1L, BIN1 +254 more	Copy number loss	See cases	GPathogenic
Select item 60184	GRCh38/hg38 2q14.1-21.3(chr2:118086324-134964738)x1	ACMSD, AMER3 +391 more	Copy number loss	See cases	GPathogenic

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Links from Gene

Items: 41