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.
Ischemia
,
Liver
,
Neocentromeres
,
Lipitor
,
rs4950928
,
ERBB2
,
T cell differentiation
)
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
chromosome 1
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
OMIM - Unspecified immunity deficiency
Acute myeloid leukemia by karyotype and by discrete mutation
Induced pluripotent stem cells (iPSC) from DNMT3B mutant ICF-1 syndrome patients
Explore Curated Studies Results
Literature
Most Relevant Literature
Characterization and Gene Mapping of an Open-Glume Oryza sativa L. Mutant.
Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1.
Evaluation of the Oncomine Comprehensive Assay v3 panel for the detection of 1p/19q codeletion in ol…
Remnants of SIRE1 retrotransposons in human genome?
Spatial metabolic heterogeneity of oligodendrogliomas at single-cell resolution.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Lenalidomide in Subject With Low and Intermediate-1 Risk MDS and Without Chromosome 5 Abnormality.
Chromosome 18 Clinical Research Center
Prospective Study to Assess Medical Performance of Optical Mapping and Long Read Sequencing in Detec…
The Clinical Study of Sex Chromosome Variants
Trisomy of Chromosome 21 Diagnosis by High Output Sequencing
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ