UCSC Genome Browser on Human (GRCh37/hg19)
Move Zoom in Zoom out
chr21:33,031,597-33,041,570 9,974 bp.
  
-   Mapping and Sequencing
Base Position
p14 Fix Patches
p14 Alt Haplotypes
Assembly
BAC End Pairs
BU ORChID
Chromosome Band
deCODE Recomb
ENCODE Pilot
Exome Probesets
FISH Clones
Fosmid End Pairs
Gap
GC Percent
GRC Incident
GRC Map Contigs
Hg18 Diff
Hg38 Diff
Hi Seq Depth
INSDC
liftOver & ReMap
LRG Regions
Map Contigs
Mappability
Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
STS Markers
+   Genes and Gene Predictions
-   Phenotype and Literature
OMIM
Publications
AbSplice Scores
CADD 1.6
new CADD 1.7
new ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC Regions
COVID Data
DECIPHER CNVs
DECIPHER SNVs
Development Delay
Dosage Sensitivity
GAD View
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
Haploinsufficiency
HGMD public
Lens Patents
LOVD Variants
MGI Mouse QTL
Orphanet
PanelApp
Polygenic Risk Scores
Prediction Scores
REVEL Scores
RGD Human QTL
RGD Rat QTL
SNPedia
new SpliceAI
UniProt Variants
Variants in Papers
Web Sequences
+   mRNA and EST
-   Expression
GTEx Gene V8
Allen Brain
Burge RNA-seq
CSHL Small RNA-seq
ENC Exon Array
ENC ProtGeno
ENC RNA-seq
EPDnew Promoters
Affy Archive
GIS RNA PET
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
Illumina WG-6
PeptideAtlas
qPCR Primers
RIKEN CAGE Loc
Sestan Brain
+   Regulation
+   Comparative Genomics
+   Neandertal Assembly and Analysis
+   Denisova Assembly and Analysis
+   Variation
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
NumtS Sequence
Segmental Dups
Self Alignment
Simple Repeats
WM + SDust
Invisible link