Variant report

Variant	nsv963876
Chromosome Location	chr2:77634291-77638298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 152 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551424430	chr2:77634294-77634295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564969663	chr2:77634305-77634306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545234421	chr2:77634401-77634402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74924822	chr2:77634411-77634412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372268766	chr2:77634431-77634432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547233918	chr2:77634575-77634576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567476602	chr2:77634627-77634628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536124593	chr2:77634630-77634631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569482099	chr2:77634633-77634634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549649026	chr2:77634637-77634638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191967409	chr2:77634650-77634651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538647872	chr2:77634664-77634665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184386326	chr2:77634714-77634715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200524840	chr2:77634760-77634761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567287708	chr2:77634761-77634762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570701483	chr2:77634763-77634764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189269300	chr2:77634783-77634784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112195602	chr2:77634785-77634786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575393262	chr2:77634794-77634795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573073082	chr2:77634797-77634798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572411213	chr2:77634822-77634823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528853395	chr2:77634827-77634828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534644309	chr2:77634831-77634832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535124237	chr2:77634844-77634845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199895931	chr2:77634845-77634846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527993660	chr2:77634846-77634847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111571700	chr2:77634853-77634854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554834882	chr2:77634900-77634901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557424606	chr2:77634913-77634914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576105893	chr2:77634983-77634984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543686171	chr2:77635008-77635009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149221612	chr2:77635026-77635027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563947631	chr2:77635047-77635048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367765564	chr2:77635090-77635091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs151307021	chr2:77635271-77635272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545011123	chr2:77635310-77635311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181975841	chr2:77635320-77635321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139368928	chr2:77635372-77635373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541137764	chr2:77635390-77635391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75075842	chr2:77635417-77635418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529877356	chr2:77635479-77635480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184341257	chr2:77635487-77635488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73942710	chr2:77635488-77635489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532285940	chr2:77635516-77635517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375278473	chr2:77635562-77635563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1796454	chr2:77635569-77635570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534772363	chr2:77635620-77635621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80056371	chr2:77635621-77635622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs694136	chr2:77635684-77635685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs144950520	chr2:77635722-77635723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77633200-77640200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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