Variant report

Variant	nsv972067
Chromosome Location	chr11:106694843-106698001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 130 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562470529	chr11:106694867-106694868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533055603	chr11:106694939-106694940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551205527	chr11:106694979-106694980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6588929	chr11:106695037-106695038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370217291	chr11:106695050-106695051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184549756	chr11:106695067-106695068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549476590	chr11:106695091-106695092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567617891	chr11:106695202-106695203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189333988	chr11:106695208-106695209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556573419	chr11:106695217-106695218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578261541	chr11:106695255-106695256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71488228	chr11:106695283-106695284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554464863	chr11:106695317-106695318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145332891	chr11:106695382-106695383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182029719	chr11:106695396-106695397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561857636	chr11:106695412-106695413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573632891	chr11:106695451-106695452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185030951	chr11:106695469-106695470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562137297	chr11:106695477-106695478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532728822	chr11:106695507-106695508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200258002	chr11:106695512-106695513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202070656	chr11:106695514-106695515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199545274	chr11:106695515-106695516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560161382	chr11:106695539-106695540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527494886	chr11:106695600-106695601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548887975	chr11:106695648-106695649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531688187	chr11:106695652-106695653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567772917	chr11:106695672-106695673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77535954	chr11:106695697-106695698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191152177	chr11:106695718-106695719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571899019	chr11:106695734-106695735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538986383	chr11:106695743-106695744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554468811	chr11:106695750-106695751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566227404	chr11:106695769-106695770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570954853	chr11:106695834-106695835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534258284	chr11:106695863-106695864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547947327	chr11:106695864-106695865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573721228	chr11:106695873-106695874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181193999	chr11:106695892-106695893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186646014	chr11:106695914-106695915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12800415	chr11:106695921-106695922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs10890599	chr11:106695944-106695945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs12800579	chr11:106695953-106695954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560430271	chr11:106695965-106695966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527567390	chr11:106695978-106695979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542852380	chr11:106696010-106696011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183073468	chr11:106696038-106696039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555801203	chr11:106696044-106696045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186295207	chr11:106696102-106696103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550299555	chr11:106696115-106696116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106689600-106699800	Weak transcription	Fetal Heart	heart
2	chr11:106694600-106699200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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