UCSC Genome Browser on Human Dec. 2013 (GRCh38/hg38) Assembly
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chr17:10,469,347-10,587,413 118,067 bp.
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-   Mapping and Sequencing
Base Position
Fix Patches
Alt Haplotypes
Assembly
Centromeres
Chromosome Band
Clone Ends
Exome Probesets
FISH Clones
Gap
GC Percent
GRC Contigs
GRC Incident
Hg19 Diff
Hg19 Mapping
INSDC
LRG Regions
Mappability
RefSeq Acc
Restr Enzymes
Scaffolds
Short Match
STS Markers
+   Genes and Gene Predictions
-   Phenotype and Literature
OMIM Alleles
CADD
Cancer Gene Expr
ClinGen
deprecated ClinGen CNVs
ClinVar Variants
Coriell CNVs
COSMIC Regions
Development Delay
Gene Interactions
GeneReviews
GWAS Catalog
HGMD Variants
LOVD Variants
OMIM Cyto Loci
OMIM Genes
new REVEL Scores
SNPedia
TCGA Pan-Cancer
UniProt Variants
Variants in Papers
-   COVID-19
COVID GWAS v4
COVID GWAS v3
Rare Harmful Vars
+   mRNA and EST
-   Expression
GTEx Gene V8
new Affy Archive
EPDnew Promoters
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
miRNA Tissue Atlas
+   Regulation
+   Comparative Genomics
+   Variation
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
RepeatMasker Viz.
Segmental Dups
Self Chain
Simple Repeats
WM + SDust