Variant report

Variant	nsv441751
Chromosome Location	chr2:35064073-35066670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 132 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558345333	chr2:35064080-35064081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571827444	chr2:35064085-35064086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562935364	chr2:35064094-35064095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540589414	chr2:35064115-35064116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560559967	chr2:35064161-35064162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573947682	chr2:35064201-35064202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80020444	chr2:35064219-35064220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530526442	chr2:35064223-35064224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563238340	chr2:35064250-35064251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531797898	chr2:35064280-35064281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545612050	chr2:35064301-35064302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76064465	chr2:35064309-35064310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527805190	chr2:35064328-35064329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113969409	chr2:35064351-35064352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567669651	chr2:35064365-35064366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530157026	chr2:35064366-35064367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549789141	chr2:35064382-35064383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569960950	chr2:35064394-35064395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538423975	chr2:35064401-35064402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557706754	chr2:35064404-35064405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371969557	chr2:35064409-35064410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189713241	chr2:35064418-35064419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374867379	chr2:35064420-35064421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192948999	chr2:35064431-35064432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141302644	chr2:35064442-35064443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369247498	chr2:35064448-35064449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111474522	chr2:35064485-35064486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139631405	chr2:35064493-35064494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556559528	chr2:35064532-35064533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185200162	chr2:35064550-35064551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78145011	chr2:35064588-35064589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565491391	chr2:35064620-35064621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527743129	chr2:35064623-35064624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190525362	chr2:35064673-35064674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181863689	chr2:35064688-35064689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568765118	chr2:35064698-35064699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550168730	chr2:35064735-35064736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534775083	chr2:35064751-35064752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569813495	chr2:35064826-35064827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116739478	chr2:35064840-35064841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145222531	chr2:35064844-35064845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552794857	chr2:35064866-35064867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186071339	chr2:35064952-35064953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554229077	chr2:35064990-35064991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147200524	chr2:35065002-35065003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78722395	chr2:35065007-35065008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188188829	chr2:35065018-35065019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535772452	chr2:35065020-35065021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576622097	chr2:35065074-35065075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545689724	chr2:35065089-35065090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35057200-35080400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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