Variant report

Variant	nsv511663
Chromosome Location	chrX:154916845-154939018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 1 )

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs669237	chrX:154916845-154916846	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369489556	chrX:154916869-154916870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145742782	chrX:154916986-154916987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374100597	chrX:154917002-154917003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112307193	chrX:154917010-154917011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370080026	chrX:154917250-154917251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138549275	chrX:154917357-154917358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191384023	chrX:154917476-154917477	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:1)

Disease	PMID	Source
Olfactory neuroblastoma	18408657	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154916400-154917000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chrX:154917000-154917600	Enhancers	Hela-S3	cervix

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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