Variant report

Variant	nsv964515
Chromosome Location	chr21:15327370-15330176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 183 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:183 , 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	rs531453386	chr21:15327380-15327381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190156506	chr21:15327395-15327396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35714031	chr21:15327429-15327430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570914544	chr21:15327479-15327480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2822318	chr21:15327490-15327491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369231829	chr21:15327491-15327492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35337936	chr21:15327512-15327513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375888168	chr21:15327515-15327516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35866701	chr21:15327534-15327535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567518603	chr21:15327568-15327569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34160718	chr21:15327573-15327574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187352976	chr21:15327589-15327590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556605010	chr21:15327596-15327597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34512104	chr21:15327602-15327603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34883981	chr21:15327636-15327637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576425186	chr21:15327637-15327638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145904120	chr21:15327650-15327651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558943802	chr21:15327668-15327669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572478408	chr21:15327690-15327691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35667747	chr21:15327692-15327693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34329550	chr21:15327694-15327695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35126238	chr21:15327710-15327711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540523252	chr21:15327731-15327732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34212171	chr21:15327747-15327748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs36054511	chr21:15327751-15327752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543474858	chr21:15327762-15327763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560473036	chr21:15327780-15327781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138301075	chr21:15327782-15327783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563560360	chr21:15327799-15327800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542425633	chr21:15327809-15327810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36152863	chr21:15327816-15327817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36154758	chr21:15327825-15327826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149616697	chr21:15327834-15327835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531261297	chr21:15327837-15327838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs36166598	chr21:15327847-15327848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551071941	chr21:15327860-15327861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs36176618	chr21:15327880-15327881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189380074	chr21:15327903-15327904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527334863	chr21:15327913-15327914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113064700	chr21:15327919-15327920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs36178091	chr21:15327961-15327962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547661202	chr21:15327978-15327979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11700508	chr21:15327980-15327981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536968262	chr21:15327983-15327984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550079015	chr21:15327984-15327985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs36182025	chr21:15327993-15327994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs36174863	chr21:15328020-15328021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148349980	chr21:15328061-15328062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3119552	chr21:15328067-15328068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3119553	chr21:15328101-15328102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15310400-15347400	Weak transcription	Dnd41	blood

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