Variant report

Variant	nsv825798
Chromosome Location	chr11:25981364-25982166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530688194	chr11:25981391-25981392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191843608	chr11:25981404-25981405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564171986	chr11:25981405-25981406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139086212	chr11:25981440-25981441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12287905	chr11:25981442-25981443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs529030744	chr11:25981443-25981444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535683264	chr11:25981526-25981527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551162646	chr11:25981611-25981612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs202108730	chr11:25981668-25981669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377138825	chr11:25981669-25981670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569595932	chr11:25981685-25981686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149625916	chr11:25981726-25981727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558474125	chr11:25981768-25981769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576954724	chr11:25981772-25981773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72406849	chr11:25981786-25981787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112345621	chr11:25981787-25981788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547547927	chr11:25981788-25981789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs328465	chr11:25981799-25981800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs60640095	chr11:25981819-25981820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1973324	chr11:25981849-25981850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551129521	chr11:25981871-25981872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572109025	chr11:25981892-25981893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72199199	chr11:25981998-25981999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201036224	chr11:25982009-25982010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541679387	chr11:25982028-25982029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs328466	chr11:25982048-25982049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs167878	chr11:25982105-25982106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs117304655	chr11:25982135-25982136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2583450	chr11:25982137-25982138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184303277	chr11:25982163-25982164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:25974400-25989400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:25975800-25982400	Weak transcription	Fetal Kidney	kidney
3	chr11:25979400-25988600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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