ClinVar (all) for Orgtrack (Select 505240) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 424862	GRCh38/hg38 16p11.2(chr16:29662633-30179247)x3		Copy number gain	See cases	GPathogenic
Select item 424857	GRCh38/hg38 16p11.2(chr16:29581462-30179247)x3		Copy number gain	See cases	GPathogenic
Select item 193029	NCBI36/hg18 4q13.2(chr4:69085386-69688461)x1		Copy number loss	See cases	GBenign
Select item 161085	GRCh38/hg38 11p15.5(chr11:196966-244236)x1	BET1L, CIMAP1A +8 more	Copy number loss	See cases	GUncertain significance
Select item 161083	GRCh38/hg38 14q32.33(chr14:106112755-106318409)x3	IGH, IGHV1-18 +12 more	Copy number gain	See cases	GBenign
Select item 161082	GRCh38/hg38 9q34.3(chr9:136323974-138014606)x1	LOC130003070, LOC130003071 +283 more	Copy number loss	See cases	GPathogenic
Select item 161081	GRCh38/hg38 15q11.2(chr15:22655582-23066575)x1	CYFIP1, LOC112272575 +18 more	Copy number loss	See cases	GUncertain significance
Select item 161078	GRCh37/hg19 1q21.2(chr1:149041013-149699420)x3	FAM72C, PPIAL4C +1 more	Copy number gain	See cases	GBenign
Select item 161077	GRCh38/hg38 9p24.3(chr9:204193-332515)x1	DOCK8, DOCK8-AS1 +7 more	Copy number loss	See cases	GUncertain significance
Select item 161076	GRCh38/hg38 15q13.2-13.3(chr15:30438310-32569425)x1	ARHGAP11B, ARHGAP11B-DT +35 more	Copy number loss	See cases	GPathogenic
Select item 161075	GRCh38/hg38 16p13.11-12.3(chr16:15457445-18047194)x3	LOC126862300, LOC126862301 +64 more	Copy number gain	See cases	GUncertain significance
Select item 161074	GRCh38/hg38 20p13(chr20:89939-1852477)x1	ANGPT4, C20orf202 +104 more	Copy number loss	See cases	GPathogenic
Select item 161072	GRCh38/hg38 15q11.2(chr15:22655582-23066575)x1	CYFIP1, LOC112272575 +18 more	Copy number loss	See cases	GUncertain significance
Select item 161071	GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3	ABCG4, ACAD8 +764 more	Copy number gain	See cases	GPathogenic
Select item 161070	GRCh38/hg38 8p23.1(chr8:7514108-8222398)x3	DEFB103A, DEFB104A +28 more	Copy number gain	See cases	GBenign
Select item 161069	GRCh38/hg38 2q13(chr2:110104900-110371270)x3	LIMS4, LOC126806305 +8 more	Copy number gain	See cases	GBenign
Select item 161067	GRCh38/hg38 6p25.3(chr6:266079-339802)x3	DUSP22, LOC126859546 +20 more	Copy number gain	See cases	GBenign
Select item 161066	GRCh38/hg38 4q34.3-35.1(chr4:181579626-186100199)x1	ACSL1, ANKRD37 +193 more	Copy number loss	See cases	GPathogenic
Select item 161065	GRCh37/hg19 Yp11.31-q12(chrY:2654852-59031480)x2	AMELY, BPY2 +81 more	Copy number gain	See cases	GPathogenic
Select item 161064	GRCh38/hg38 7p21.3(chr7:10610069-11290160)x3	LOC100131472, LOC110120772 +11 more	Copy number gain	See cases	GUncertain significance
Select item 161063	GRCh38/hg38 11q11-12.1(chr11:55319519-56212930)x3	LOC126861207, OR10AG1 +27 more	Copy number gain	See cases	GBenign
Select item 161062	GRCh38/hg38 19q13.32(chr19:46434490-46831000)x3	CALM3, DACT3 +46 more	Copy number gain	See cases	GUncertain significance
Select item 161061	GRCh38/hg38 4q22.1-22.2(chr4:92513191-94071223)x3	ATOH1, GRID2 +6 more	Copy number gain	See cases	GUncertain significance
Select item 161060	GRCh38/hg38 7q11.22(chr7:70891025-71072442)x3	LOC129998575	Copy number gain	See cases	GUncertain significance
Select item 161059	GRCh38/hg38 22q13.31(chr22:46183346-46791748)x3	CDPF1, CELSR1 +57 more	Copy number gain	See cases	GUncertain significance
Select item 161058	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	LOC126860732, LOC126860733 +514 more	Copy number loss	See cases	GPathogenic
Select item 161057	GRCh38/hg38 4p16.3(chr4:72555-2108607)x1	ATP5ME, CPLX1 +134 more	Copy number loss	See cases	GPathogenic
Select item 161056	GRCh38/hg38 13q33.3-34(chr13:107918132-114327173)x1	ABHD13, ADPRHL1 +286 more	Copy number loss	See cases	GPathogenic
Select item 161055	GRCh38/hg38 22q13.33(chr22:50658268-50739836)x1	ACR, LOC105373100 +3 more	Copy number loss	See cases	GPathogenic
Select item 161054	GRCh38/hg38 Xq28(chrX:156001591-156022206)x0	IL9R, WASIR1	Copy number loss	See cases	GBenign
Select item 161053	GRCh38/hg38 Xq28(chrX:156001591-156022206)x1	IL9R, WASIR1	Copy number loss	See cases	GBenign
Select item 161052	GRCh38/hg38 3p26.3-26.2(chr3:2220949-2920945)x3	CNTN4, LOC107522028 +5 more	Copy number gain	See cases	GUncertain significance
Select item 161051	GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1	LOC129935965, LOC129935966 +455 more	Copy number loss	See cases	GPathogenic
Select item 161050	GRCh38/hg38 15q11.2(chr15:22726969-23066575)x3	CYFIP1, LOC112272575 +17 more	Copy number gain	See cases	GUncertain significance
Select item 161049	GRCh38/hg38 22q11.21(chr22:18339130-20354644)x1	ARVCF, C22orf39 +120 more	Copy number loss	See cases	GPathogenic
Select item 161048	GRCh38/hg38 22q11.21(chr22:18339130-21454720)x1	AIFM3, ARVCF +195 more	Copy number loss	See cases	GPathogenic
Select item 161047	GRCh38/hg38 Xq27.1-27.2(chrX:141160282-141469623)x0	LDOC1, SPANXC	Copy number loss	See cases	GUncertain significance
Select item 161046	GRCh38/hg38 2q13-14.1(chr2:110684553-112308202)x3	ACOXL, ACOXL-AS1 +47 more	Copy number gain	See cases	GUncertain significance
Select item 161043	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x1	AGAP10, AGAP9 +34 more	Copy number loss	See cases	GBenign
Select item 161042	GRCh38/hg38 22q11.21(chr22:18178957-21151128)x3	AIFM3, ARVCF +186 more	Copy number gain	See cases	GPathogenic
Select item 161041	GRCh38/hg38 17q12(chr17:36357258-37889296)x1	AATF, ACACA +35 more	Copy number loss	See cases	GPathogenic
Select item 161040	GRCh38/hg38 1q41(chr1:215206760-222004068)x1	BPNT1, C1orf115 +138 more	Copy number loss	See cases	GPathogenic
Select item 161038	GRCh38/hg38 8p23.3-23.1(chr8:241530-7895064)x1	AGPAT5, ANGPT2 +166 more	Copy number loss	See cases	GPathogenic
Select item 161037	GRCh38/hg38 8p23.2-21.1(chr8:2475295-27504279)x1	ADAM28, ADAM7 +773 more	Copy number loss	See cases	GPathogenic
Select item 161036	GRCh38/hg38 8p23.3-23.1(chr8:241530-7895064)x3	AGPAT5, ANGPT2 +166 more	Copy number gain	See cases	GPathogenic
Select item 161035	GRCh38/hg38 8p23.3(chr8:244617-2017223)x1	ARHGEF10, CLN8 +46 more	Copy number loss	See cases	GPathogenic
Select item 161034	GRCh38/hg38 5p15.33-15.1(chr5:49978-15678451)x1	ADAMTS16, ADAMTS16-DT +461 more	Copy number loss	See cases	GPathogenic
Select item 161033	GRCh38/hg38 8p23.1-11.21(chr8:12609975-42085703)x3	LOC129999967, LOC129999968 +870 more	Copy number gain	See cases	GPathogenic
Select item 161031	GRCh38/hg38 19q13.2-13.31(chr19:42738643-43237158)x1	LOC284344, PSG1 +10 more	Copy number loss	See cases	GBenign
Select item 161030	GRCh38/hg38 3p26.3(chr3:868334-1341994)x1	CNTN6, LOC126806587	Copy number loss	See cases	GUncertain significance
Select item 161029	GRCh38/hg38 19q13.2-13.31(chr19:42738643-43237158)x3	LOC284344, PSG1 +10 more	Copy number gain	See cases	GBenign
Select item 161028	GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3	ACOD1, AKAP11 +992 more	Copy number gain	See cases	GPathogenic
Select item 161027	GRCh38/hg38 6q27(chr6:167963663-168157303)x3	AFDN, FRMD1 +5 more	Copy number gain	See cases	GBenign
Select item 161026	GRCh38/hg38 2q37.3(chr2:241988449-242065208)x1	LINC01237, LINC01880 +2 more	Copy number loss	See cases	GBenign
Select item 161024	GRCh38/hg38 22q11.22(chr22:21981871-22202339)x3	IGL, IGLV11-55 +18 more	Copy number gain	See cases	GBenign
Select item 161023	GRCh38/hg38 2q13(chr2:110104900-110611314)x3	LIMS4, LINC01106 +11 more	Copy number gain	See cases	GBenign
Select item 161022	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 161021	GRCh38/hg38 7p22.3(chr7:101528-227833)x3	FAM20C, LINC03014 +3 more	Copy number gain	See cases	GBenign
Select item 161020	GRCh38/hg38 4p16.3(chr4:72555-113701)x3	ZNF595	Copy number gain	See cases	GBenign
Select item 161019	GRCh38/hg38 8p23.1-11.1(chr8:12728904-43673207)x3	LOC130000303, LOC130000304 +922 more	Copy number gain	See cases	GPathogenic
Select item 161018	GRCh38/hg38 16p12.2(chr16:21463739-21826230)x1	IGSF6, LOC101927814 +11 more	Copy number loss	See cases	GUncertain significance
Select item 161015	GRCh38/hg38 2q13(chr2:110104900-110207160)x1	LOC126806305, LOC126806306 +2 more	Copy number loss	See cases	GBenign
Select item 161014	GRCh38/hg38 17q21.31(chr17:45629520-46111134)x1	CRHR1, KANSL1 +9 more	Copy number loss	See cases	GPathogenic
Select item 161013	GRCh38/hg38 2p11.2(chr2:87148954-87705899)x1	CYTOR, LINC01943 +4 more	Copy number loss	See cases	GBenign
Select item 161012	GRCh38/hg38 8p23.1(chr8:7411297-8222398)x1	DEFB103A, DEFB103B +35 more	Copy number loss	See cases	GBenign
Select item 161011	GRCh38/hg38 8p23.1(chr8:7411297-8222398)x3	DEFB103A, DEFB103B +35 more	Copy number gain	See cases	GBenign
Select item 161010	GRCh38/hg38 8p23.1(chr8:7411297-7895064)x1	DEFB103A, DEFB103B +26 more	Copy number loss	See cases	GBenign
Select item 161009	GRCh38/hg38 16p11.2-11.1(chr16:35247671-35492978)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 161008	GRCh38/hg38 10q26.3(chr10:133440535-133564028)x1	CYP2E1, LOC110599585 +8 more	Copy number loss	See cases	GBenign
Select item 161007	GRCh38/hg38 14q32.33(chr14:106450995-106714110)x3	IGH, IGHV1-45 +12 more	Copy number gain	See cases	GBenign
Select item 161006	GRCh38/hg38 15q13.3(chr15:31738809-32217725)x3	CHRNA7, LOC125078053 +3 more	Copy number gain	See cases	GBenign
Select item 161005	GRCh38/hg38 12q24.33(chr12:129325762-129943507)x3	LOC126861687, LOC126861688 +4 more	Copy number gain	See cases	GBenign
Select item 161004	GRCh38/hg38 11q25(chr11:134511738-134841778)x3	LINC02706, LINC02714 +3 more	Copy number gain	See cases	GBenign
Select item 161003	GRCh38/hg38 1q42.2(chr1:230519755-231232066)x3	AGT, ARV1 +34 more	Copy number gain	See cases	GUncertain significance
Select item 161002	GRCh38/hg38 10q26.3(chr10:133538868-133620674)x3	CYP2E1, SYCE1	Copy number gain	See cases	GBenign
Select item 161001	GRCh38/hg38 8p23.1(chr8:8273108-11948451)x3	BLK, C8orf74 +189 more	Copy number gain	See cases	GPathogenic
Select item 161000	GRCh38/hg38 8q11.1(chr8:46031334-46662449)x1		Copy number loss	See cases	GBenign
Select item 160998	GRCh38/hg38 22q11.23-12.1(chr22:25299502-25507576)x1	LOC106780824, LOC125424402 +9 more	Copy number loss	See cases	GBenign
Select item 160997	GRCh38/hg38 6p25.3(chr6:259528-389482)x1	DUSP22, LOC126859546 +28 more	Copy number loss	See cases	GBenign
Select item 160996	GRCh38/hg38 10q25.1(chr10:108680957-109329708)x1	LINC02661, LOC126861035 +7 more	Copy number loss	See cases	GUncertain significance
Select item 160995	GRCh38/hg38 10q26.3(chr10:133440535-133564028)x3	CYP2E1, LOC110599585 +8 more	Copy number gain	See cases	GBenign
Select item 160993	GRCh38/hg38 6p25.3(chr6:259528-293493)x3	DUSP22, LOC129995536 +2 more	Copy number gain	See cases	GBenign
Select item 160992	GRCh38/hg38 6p25.3(chr6:259528-339802)x1	DUSP22, LOC126859546 +20 more	Copy number loss	See cases	GBenign
Select item 160991	GRCh38/hg38 6p25.3(chr6:259528-339802)x3	DUSP22, LOC126859546 +20 more	Copy number gain	See cases	GBenign
Select item 160990	GRCh38/hg38 6p25.3(chr6:259528-307998)x3	DUSP22, LOC129995536 +6 more	Copy number gain	See cases	GBenign
Select item 160989	GRCh38/hg38 15q11.2-13.1(chr15:23319714-30361733)x3	APBA2, ATP10A +170 more	Copy number gain	See cases	GPathogenic
Select item 160988	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 160987	GRCh38/hg38 16p13.11-12.3(chr16:15310595-18212997)x3	ABCC1, ABCC6 +66 more	Copy number gain	See cases	GUncertain significance
Select item 160986	GRCh38/hg38 22q11.21(chr22:20726972-21151128)x3	AIFM3, CRKL +34 more	Copy number gain	See cases	GPathogenic
Select item 160985	GRCh38/hg38 20q13.33(chr20:63199020-64277321)x3	ABHD16B, ARFGAP1 +177 more	Copy number gain	See cases	GPathogenic
Select item 160984	GRCh38/hg38 22q11.21(chr22:18339130-21086225)x3	AIFM3, ARVCF +185 more	Copy number gain	See cases	GPathogenic
Select item 160983	GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1	LOC130067918, LOC130067919 +2633 more	Copy number loss	See cases	GPathogenic
Select item 160981	GRCh38/hg38 22q13.33(chr22:50368887-50599372)x3	ADM2, CHKB +52 more	Copy number gain	See cases	GUncertain significance
Select item 160980	GRCh38/hg38 9p24.3(chr9:204193-381489)x3	DOCK8, DOCK8-AS1 +7 more	Copy number gain	See cases	GUncertain significance
Select item 160979	GRCh38/hg38 2q37.3(chr2:241988449-242126245)x1	LINC01237, LINC01880 +4 more	Copy number loss	See cases	GBenign
Select item 160975	GRCh38/hg38 2p25.3(chr2:30341-507042)x3	ACP1, ALKAL2 +18 more	Copy number gain	See cases	GPathogenic
Select item 160974	GRCh38/hg38 5q23.1(chr5:117766849-118700657)x1	LINC02147, LINC02148 +7 more	Copy number loss	See cases	GUncertain significance
Select item 160973	GRCh38/hg38 16p13.11(chr16:14954894-16100721)x3	ABCC1, BMERB1 +33 more	Copy number gain	See cases	GUncertain significance
Select item 160972	GRCh38/hg38 15q13.2-13.3(chr15:30662523-32217725)x3	CHRNA7, FAN1 +23 more	Copy number gain	See cases	GUncertain significance
Select item 160971	GRCh38/hg38 15q11.2-13.1(chr15:22358243-28481444)x3	SNORD107, SNORD108 +171 more	Copy number gain	See cases	GPathogenic

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