"ISCA site 1"[submitter] AND "CNTN4"[gene] - ClinVar

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Items: 90

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155626	GRCh38/hg38 3p26.3-26.2(chr3:20213-3244317)x1	CHL1, CHL1-AS1 +37 more	Copy number loss	See cases	GUncertain significance
Select item 154175	GRCh38/hg38 3p26.3-25.3(chr3:20213-9362037)x1	ARL8B, BHLHE40 +172 more	Copy number loss	See cases	GPathogenic
Select item 153284	GRCh38/hg38 3p26.3-25.3(chr3:20213-11221602)x1	ARL8B, ARPC4 +286 more	Copy number loss	See cases	GPathogenic
Select item 155258	GRCh38/hg38 3p26.3-25.3(chr3:32241-10323124)x1	ARL8B, ARPC4 +263 more	Copy number loss	See cases	GPathogenic
Select item 155106	GRCh38/hg38 3p26.3-25.3(chr3:32241-10631310)x1	ARL8B, ARPC4 +271 more	Copy number loss	See cases	GPathogenic
Select item 152808	GRCh38/hg38 3p26.3-25.3(chr3:32241-8165256)x3	ARL8B, BHLHE40 +139 more	Copy number gain	See cases	GLikely pathogenic
Select item 152256	GRCh38/hg38 3p26.3-25.3(chr3:32241-9066287)x1	ARL8B, BHLHE40 +162 more	Copy number loss	See cases	GPathogenic
Select item 151534	GRCh38/hg38 3p26.3-25.3(chr3:32241-9574994)x1	ARL8B, BHLHE40 +184 more	Copy number loss	See cases	GPathogenic
Select item 150610	GRCh38/hg38 3p26.3-26.2(chr3:32241-3355776)x1	CHL1, CHL1-AS1 +36 more	Copy number loss	See cases	GLikely pathogenic
Select item 150393	GRCh38/hg38 3p26.3-25.3(chr3:32241-9469506)x1	ARL8B, BHLHE40 +181 more	Copy number loss	See cases	GPathogenic
Select item 150031	GRCh38/hg38 3p26.3-25.1(chr3:32241-13613818)x3	ARL8B, ARPC4 +406 more	Copy number gain	See cases	GPathogenic
Select item 149555	GRCh38/hg38 3p26.3-26.1(chr3:32241-6065999)x1	ARL8B, BHLHE40 +126 more	Copy number loss	See cases	GPathogenic
Select item 149331	GRCh38/hg38 3p26.3-25.3(chr3:32241-11379835)x1	ARL8B, ARPC4 +291 more	Copy number loss	See cases	GPathogenic
Select item 149236	GRCh38/hg38 3p26.3-26.1(chr3:32241-7056717)x1	LOC129936092, LOC129936093 +134 more	Copy number loss	See cases	GPathogenic
Select item 149085	GRCh38/hg38 3p26.3-25.2(chr3:32241-12681483)x1	ARL8B, ARPC4 +331 more	Copy number loss	See cases	GPathogenic
Select item 148942	GRCh38/hg38 3p26.3-24.1(chr3:32241-30064208)x3	ANKRD28, ARL8B +799 more	Copy number gain	See cases	GPathogenic
Select item 148876	GRCh38/hg38 3p26.3-24.3(chr3:32241-20334387)x3	LOC129936198, LOC129936199 +647 more	Copy number gain	See cases	GPathogenic
Select item 154452	GRCh38/hg38 3p26.3-26.1(chr3:52266-5966084)x3	ARL8B, BHLHE40 +126 more	Copy number gain	See cases	GPathogenic
Select item 148015	GRCh38/hg38 3p26.3-25.3(chr3:52266-9450310)x1	ARL8B, BHLHE40 +181 more	Copy number loss	See cases	GPathogenic
Select item 147496	GRCh38/hg38 3p26.3-26.1(chr3:52266-6277604)x1	ARL8B, BHLHE40 +126 more	Copy number loss	See cases	GPathogenic
Select item 146281	GRCh38/hg38 3p26.3-26.1(chr3:52266-5138262)x1	ARL8B, BHLHE40 +102 more	Copy number loss	See cases	GPathogenic
Select item 153415	GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3	ACAA1, ACVR2B +1111 more	Copy number gain	See cases	GPathogenic
Select item 155639	GRCh38/hg38 3p26.3-25.3(chr3:688897-11051142)x1	ARL8B, ARPC4 +274 more	Copy number loss	See cases	GPathogenic
Select item 146294	GRCh38/hg38 3p26.3(chr3:868334-2301227)x3	CNTN4, CNTN4-AS2 +5 more	Copy number gain	See cases	GUncertain significance
Select item 152070	GRCh38/hg38 3p26.3(chr3:1172223-2177100)x1	CNTN4, CNTN4-AS2 +4 more	Copy number loss	See cases	GUncertain significance
Select item 155091	GRCh38/hg38 3p26.3(chr3:1175928-2130831)x3	CNTN4, CNTN4-AS2 +4 more	Copy number gain	See cases	GUncertain significance
Select item 152112	GRCh38/hg38 3p26.3(chr3:1196033-2127526)x3	CNTN4, CNTN4-AS2 +4 more	Copy number gain	See cases	GUncertain significance
Select item 153668	GRCh38/hg38 3p26.3(chr3:1275175-2359367)x3	CNTN4, CNTN4-AS2 +4 more	Copy number gain	See cases	GUncertain significance
Select item 146432	GRCh38/hg38 3p26.3(chr3:1497564-2221008)x3	CNTN4, CNTN4-AS2 +2 more	Copy number gain	See cases	GUncertain significance
Select item 147822	GRCh38/hg38 3p26.3(chr3:1699229-2368860)x1	CNTN4, CNTN4-AS2 +2 more	Copy number loss	See cases	GUncertain significance
Select item 154508	GRCh38/hg38 3p26.3(chr3:1780588-2221008)x3	CNTN4, CNTN4-AS2	Copy number gain	See cases	GUncertain significance
Select item 155170	GRCh38/hg38 3p26.3(chr3:1794929-2728825)x3	CNTN4, CNTN4-AS2 +6 more	Copy number gain	See cases	GUncertain significance
Select item 155175	GRCh38/hg38 3p26.3(chr3:1798595-2731479)x3	CNTN4, CNTN4-AS2 +6 more	Copy number gain	See cases	GUncertain significance
Select item 148543	GRCh38/hg38 3p26.3(chr3:1861223-2540213)x3	CNTN4, CNTN4-AS2 +5 more	Copy number gain	See cases	GLikely benign
Select item 145659	GRCh38/hg38 3p26.3(chr3:1880775-2143591)x3	CNTN4, CNTN4-AS2	Copy number gain	See cases	GUncertain significance
Select item 149284	GRCh38/hg38 3p26.3(chr3:1920995-2164995)x3	CNTN4, CNTN4-AS2	Copy number gain	See cases	Gconflicting data from submitters
Select item 148354	GRCh38/hg38 3p26.3(chr3:2017939-2528404)x3	CNTN4, CNTN4-AS2 +4 more	Copy number gain	See cases	GUncertain significance
Select item 150310	GRCh38/hg38 3p26.3(chr3:2045527-2100653)x3	CNTN4	Copy number gain	See cases	GLikely benign
Select item 155569	GRCh38/hg38 3p26.3(chr3:2049380-2753532)x1	CNTN4, CNTN4-AS2 +6 more	Copy number loss	See cases	GLikely benign
Select item 153431	GRCh38/hg38 3p26.3(chr3:2127695-2406764)x3	CNTN4, CNTN4-AS2 +2 more	Copy number gain	See cases	GUncertain significance
Select item 155593	GRCh38/hg38 3p26.3(chr3:2170633-2434666)x3	CNTN4, LOC107522028 +2 more	Copy number gain	See cases	GUncertain significance
Select item 155333	GRCh38/hg38 3p26.3(chr3:2187760-2269057)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 148443	GRCh38/hg38 3p26.3(chr3:2191308-2628718)x3	CNTN4, LOC107522028 +4 more	Copy number gain	See cases	GUncertain significance
Select item 152071	GRCh38/hg38 3p26.3(chr3:2195528-2387056)x3	CNTN4, LOC107522028 +1 more	Copy number gain	See cases	GUncertain significance
Select item 147425	GRCh38/hg38 3p26.3(chr3:2220949-2754945)x1	LOC129936037, LOC129936038 +5 more	Copy number loss	See cases	GUncertain significance
Select item 146194	GRCh38/hg38 3p26.3-26.2(chr3:2220949-2920945)x1	CNTN4, LOC107522028 +5 more	Copy number loss	See cases	GUncertain significance
Select item 155217	GRCh38/hg38 3p26.3(chr3:2232369-2443380)x3	CNTN4, LOC107522028 +2 more	Copy number gain	See cases	GUncertain significance
Select item 146360	GRCh38/hg38 3p26.3(chr3:2267324-2368860)x1	CNTN4, LOC132088944	Copy number loss	See cases	GLikely benign
Select item 150356	GRCh38/hg38 3p26.3(chr3:2289743-2342300)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 150154	GRCh38/hg38 3p26.3-26.2(chr3:2312470-2907234)x3	CNTN4, LOC107522028 +4 more	Copy number gain	See cases	GUncertain significance
Select item 151196	GRCh38/hg38 3p26.3(chr3:2370870-2598145)x1	LOC132088949, CNTN4 +3 more	Copy number loss	See cases	GUncertain significance
Select item 149557	GRCh38/hg38 3p26.3(chr3:2459369-2608200)x1	CNTN4, LOC129936036 +1 more	Copy number loss	See cases	GUncertain significance
Select item 155585	GRCh38/hg38 3p26.3-26.2(chr3:2466349-2888490)x3	CNTN4, LOC129936036 +2 more	Copy number gain	See cases	GUncertain significance
Select item 148921	GRCh38/hg38 3p26.3(chr3:2557269-2698434)x3	CNTN4, LOC129936038	Copy number gain	See cases	GUncertain significance
Select item 155381	GRCh38/hg38 3p26.3(chr3:2567532-2637831)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 153661	GRCh38/hg38 3p26.3-26.2(chr3:2621940-2836665)x1	CNTN4, LOC129936038	Copy number loss	See cases	GUncertain significance
Select item 149253	GRCh38/hg38 3p26.3-26.2(chr3:2628659-3001914)x3	CNTN4, LOC129389017 +5 more	Copy number gain	See cases	GLikely benign
Select item 149119	GRCh38/hg38 3p26.3(chr3:2683203-2787471)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 155549	GRCh38/hg38 3p26.3-26.2(chr3:2740571-3165943)x3	CNTN4, CNTN4-AS1 +15 more	Copy number gain	See cases	GUncertain significance
Select item 148726	GRCh38/hg38 3p26.3-26.2(chr3:2749924-3037155)x1	CNTN4, LOC129389017 +5 more	Copy number loss	See cases	GUncertain significance
Select item 154282	GRCh38/hg38 3p26.2(chr3:2847667-3320817)x3	CNTN4, CNTN4-AS1 +17 more	Copy number gain	See cases	GUncertain significance
Select item 153828	GRCh38/hg38 3p26.2(chr3:2875937-2920705)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 153151	GRCh38/hg38 3p26.2-26.1(chr3:2891585-5911622)x1	ARL8B, BHLHE40 +107 more	Copy number loss	See cases	GPathogenic
Select item 147406	GRCh38/hg38 3p26.2-26.1(chr3:2920886-5861108)x1	ARL8B, BHLHE40 +107 more	Copy number loss	See cases	GPathogenic
Select item 443895	GRCh37/hg19 3p26.3-26.2(chr3:2427405-2903886)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 443797	GRCh37/hg19 3p26.2-26.1(chr3:2930451-5953602)x1	ARL8B, BHLHE40 +10 more	Copy number loss	See cases	GPathogenic
Select item 443685	GRCh37/hg19 3p26.3(chr3:2276833-2300256)x1	CNTN4	Copy number loss	See cases	GLikely benign
Select item 443588	GRCh37/hg19 3p26.3(chr3:2609216-2663640)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 443586	GRCh37/hg19 3p26.3(chr3:2347812-2401051)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 443464	GRCh37/hg19 3p26.3-22.2(chr3:61891-37459464)x3	ANKRD28, APRG1 +155 more	Copy number gain	See cases	GPathogenic
Select item 443427	GRCh37/hg19 3p26.3(chr3:2372454-2387199)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 443417	GRCh37/hg19 3p26.3(chr3:2266037-2401051)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 443360	GRCh37/hg19 3p26.3-26.1(chr3:61891-7456866)x1	ARL8B, BHLHE40 +13 more	Copy number loss	See cases	GPathogenic
Select item 443328	GRCh37/hg19 3p26.3(chr3:1217612-2174323)x3	CNTN4, CNTN6	Copy number gain	See cases	GUncertain significance
Select item 443314	GRCh37/hg19 3p26.3-26.2(chr3:2309378-2813116)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 443284	GRCh37/hg19 3p26.3(chr3:2332721-2384323)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 443052	GRCh37/hg19 3p26.3-25.3(chr3:61891-8777555)x1	ARL8B, BHLHE40 +17 more	Copy number loss	See cases	GPathogenic
Select item 443032	GRCh37/hg19 3p26.3(chr3:2212703-2475508)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 442876	GRCh37/hg19 3p26.3(chr3:2412554-2621687)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 442710	GRCh37/hg19 3p26.3(chr3:1063666-2204464)x1	CNTN4, CNTN6	Copy number loss	See cases	GUncertain significance
Select item 442402	GRCh37/hg19 3p26.3-26.1(chr3:61891-4196715)x3	CHL1, CNTN4 +5 more	Copy number gain	See cases	GUncertain significance
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	CMTM6, CMTM7 +1054 more	Copy number gain	See cases	GPathogenic
Select item 442264	GRCh37/hg19 3p26.3-25.2(chr3:61891-12575409)x1	ARL8B, ARPC4 +60 more	Copy number loss	See cases	GPathogenic
Select item 442243	GRCh37/hg19 3p26.3-26.1(chr3:61891-7865381)x1	SETMAR, SUMF1 +13 more	Copy number loss	See cases	GPathogenic
Select item 442176	GRCh37/hg19 3p26.3(chr3:2282129-2465515)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 442122	GRCh37/hg19 3p26.3(chr3:2303077-2494007)x1	CNTN4	Copy number loss	See cases	GUncertain significance
Select item 442038	GRCh37/hg19 3p26.3-26.2(chr3:2625860-3083366)x3	CNTN4	Copy number gain	See cases	GUncertain significance
Select item 441705	GRCh37/hg19 3p26.3-22.3(chr3:61891-33958201)x3	TRIM71, TRNT1 +145 more	Copy number gain	See cases	GPathogenic
Select item 441682	GRCh37/hg19 3p26.3(chr3:1216168-2174323)x3	CNTN4, CNTN6	Copy number gain	See cases	GUncertain significance

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Items: 90