BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
PRKCA
,
Metabolism of xenobiotics
,
Leukemia
,
Liver
,
Avian flu virus
,
Vitamin E
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
marker chromosome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
No biogroups found
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
Acute myeloid leukemia by karyotype and by discrete mutation
Bone marrow gene expression of pediatric acute lymphoblastic leukemia
LSK cells from bone marrow of wildtype and Dp(16)1Yey/+ Down syndrome mice
B-cells (trisomic 21 or disomic 21) from iPSC from fibroblasts of patients with Down syndrome
Hematopoietic stem cells from mice with chromosome 7q22 heterozygous deletion
Explore Curated Studies Results
Literature
Most Relevant Literature
Identification of human small supernumerary marker chromosomes and discussion of its research value]…
Identification of origins of marker chromosomes using fluorescence in situ hybridization].
A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary…
Three supernumerary marker chromosomes in a patient with developmental delay, mental retardation, an…
De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lub…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Accuracy Testing of the Chromosomal Aberration and Gene Mutation Markers of the AMLProfiler
Chromosomal Instability in Ovarian Cancer
Non-Invasive Determination of Fetal Chromosome Abnormalities
Chromosome 5Q Gene Variants and Asthma-Related Traits
Relationship of Genetic Differences to the Development of Chromosome Abnormalities
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ