Search

Landmark or Region: Examples: chr7:71890181..72690180, CFTR, AC108171.3, nsv529033.
Data Source	Scroll/Zoom: Flip

Filter variants

Overview

Chromosome (overview)

Details

Disease Genes (OMIM)

Cytogenetic Bands

DGV Structural Variants (Blue:Gain;Red:Loss;Bro...

RefSeq Genes

UCSC segmental duplications

DECIPHER Genomic Disorders

Tracks

Custom Tracks

There are no tracks yet.

Clones on WGTP Array [?]	Clones on SMRT BAC Array [?]	NimbleGen 385K Whole Genome Array [?]
Agilent 244k [?]	Cytochip V3.0 [?]

ISCA Curated clinically relevant regions [?]	Disease Genes (OMIM) [?]	DECIPHER: Chromosomal Imbalance and Phenotype in Humans (Blue:Gain;Red:Loss;Brown:Complex;Black:NA) [?]
ISCA Clinical cytogenetic testing (Blue:Gain;Red:Loss;Brown:Complex;Black:NA) [?]	DECIPHER Genomic Disorders [?]

Personal Genome Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]	SNPs [?]	RepeatMasker [?]
dbRIP [?]	Recombination hotspots [?]

DGV Structural Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]	DGV Version 1 Structural Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]
Supporting Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inverison;Black:Unknown) [?]	Unannotated Studies (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]

Show grid	Image Width 600 760 980 1240	Highlight feature(s) (feature1 feature2...) Clear highlighting
Cache tracks		Highlight regions (region1:start..end region2:start..end) Clear highlighting
Show tooltips		Region Size (bp)

Genomic Variants in Human Genome (Build 36: Mar. 2006, hg18): 188.7 kbp from chr7:116,907,253..117,095,954