UCSC Genome Browser on Human (GRCh38/hg38)
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chr17:10,469,347-10,587,413 118,067 bp.
  
-   Mapping and Sequencing
Base Position
p14 Fix Patches
p14 Alt Haplotypes
Assembly
Assembly Tracks
Centromeres
Chromosome Band
Clone Ends
Exome Probesets
Gap
GC Percent
GRC Incident
Hg19 Diff
INSDC
LiftOver & ReMap
LRG Regions
Mappability
updated Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
+   Genes and Gene Predictions
-   Phenotypes, Variants, and Literature
OMIM
AlphaMissense
CADD 1.6
new CADD 1.7
Cancer Gene Expr
new CIViC
new ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
updated COSMIC
COSMIC Regions
COVID Data
new DECIPHER
Development Delay
Dosage Sensitivity
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
HGMD public
LOVD Variants
new MITOMAP
[No data-chr17]
Orphanet
PanelApp
REVEL Scores
SNPedia
new Splicing Impact
TCGA Pan-Cancer
UniProt Variants
updated Variants in Papers
+   Variation
-   Human Pangenome - HPRC
Multiple Alignment
Pairwise Alignments
Rearrangements
Short Variants
+   mRNA and EST
-   Expression
GTEx Gene V8
GTEx RNA-Seq Coverage
Affy Archive
EPDnew Promoters
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
miRNA Tissue Atlas
Single Cell Expression
+   Single Cell RNA-seq
+   Regulation
+   Comparative Genomics
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
NuMTs Sequence
RepeatMasker Viz.
Segmental Dups
Self Alignment
Simple Repeats
WM + SDust
Invisible link