Genomic Variants in Human Genome (Build 36: Mar. 2006, hg18)

Name	Type	Description	Position	Match Score
AC108171.3	Clone		chrX:151299438..151485145	n/a
AC108171.3	component		chrX:151304011..151485145	n/a

Breakpoints

All on All off

Breakpoint annotations from Lam et al (Blue:Gain;Red:Loss;Indigo:Inversion;Brown:Complex) [?]

Annotations from Conrad et al [?]

Breakpoint annotations from Pang 2012 (Blue:Gain;Red:Loss;Indigo:Inversion;Brown:Complex) [?]

CGH Arrays

All on All off

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

CN Assays

All on All off

Life Technologies TaqMan Copy Number Assays [?]

Chromosome

All on All off

Cytogenetic Bands [?]

Assembly [?]

Gap [?]

Clones

All on All off

Clone [?]

BAC End Pairs [?]

Fosmid End Pairs [?]

Disease

All on All off

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 [?]

Gene

All on All off

RefSeq Genes [?]

mRNA [?]

microRNA [?]

General

All on All off

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

SNP Arrays

All on All off

AFFY SNP Array 5.0 [?]	ILMN HumanHap 550 [?]	ILMN HumanHap 1M [?]
AFFY SNP Array 6.0 [?]	ILMN HumanHap 650Y [?]
ILMN HumanHap 300 [?]	ILMN Human 660W [?]

Segmental Duplications

All on All off

WSSD duplications [?]

UCSC segmental duplications [?]

Study Variants

All on All off

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) [?]

Overview

All on All off

Chromosome (overview)

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)

The following 2 regions match your request.

Custom Tracks

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