UCSC Genome Browser on Human (GRCh37/hg19)
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chr18:1-78,077,248 78,077,248 bp.
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-   Custom Tracks
Eczema
Hearing loss
Strabismus-1
Congenital heart dz-1
Constipation
Asthma
Cond. hearing loss
Ptosis-1
Scoliosis / Kyphosis
Nystagmus-1
Kidney abn
Holoprosencephaly
White_matter_abn
Cryptorchidism
Sacral agenesis
Cleft palate
Deafness_ auto_rec46
Myopia_auto_dom1
Tetralogy of Fallot
Pectus excavatum
Keratosis pilaris
Thyroid abn
Pituitary abn
Seizure-1
Bipolar affect dis
Arthritis-1
Autoimmune dis
Congenital cataracts
Hip dysplasia
HemiplegCerebralPalsy
Caries-1
Strabismus-2
Major affect dis
Schizophrenia-2
Caries-2
Febrile seizures,fam
Dyslexia-1
ProteinCdeficiency
Arthritis-2
HZL1
Intracranial aneurysm
Anosmia isolated
Alopecia-MR syn3
Scoliosis, pectus excav
Autism-2
Suicide
Autism-3
Virchow-Robin space
Sleepwalking
Dev Delay, Intel Dis
Autism spect-18-2
Microcephaly
Small corpus callosum
Ptosis-2
Seizure-2
Strabismus-3
Dysmyelination-1
Optic atrophy-4
Oralfacial cleft-11
HZL2
Dyslexia-2
Hypertension-1
Autism spect-18-3
Insulin-dep diabetes
ALS3
Speech dev, ID, sleep
Dandy Walker Vari
Dyslexia-3
ADHD/I
Hypertension-2
Major affect dis_18q
Type 2 diabetes
Male infertility
Ectodermal dysplasia
IgA deficiency
Atopic disorders
Chiari malform
Mood disorder
Nystagmus-2
Congenital Heart Dz-2
Kidney malform
Vertical talus
Dysmyelination-2
GrowthHormone def
Cleft abn
Macroglossia
Occipital lobes
+   Mapping and Sequencing
-   Genes and Gene Predictions
UCSC Genes
NCBI RefSeq
CCDS
CRISPR Targets
Ensembl Genes
EvoFold
Exoniphy
updated GENCODE Versions
H-Inv 7.0
HGNC
IKMC Genes Mapped
lincRNAs
LRG Transcripts
MGC Genes
Old UCSC Genes
ORFeome Clones
Other RefSeq
Pfam in UCSC Gene
Prediction Archive
Retroposed Genes
sno/miRNA
TransMap V5
tRNA Genes
UCSC Alt Events
UniProt
Vega Genes
Yale Pseudo60
-   Phenotype and Literature
Publications
CADD
ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC Regions
DECIPHER CNVs
DECIPHER SNVs
Development Delay
GAD View
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
Haploinsufficiency
HGMD Variants
Lens Patents
LOVD Variants
MGI Mouse QTL
OMIM Alleles
OMIM Cyto Loci
OMIM Genes
Orphanet
PanelApp
REVEL Scores
RGD Human QTL
RGD Rat QTL
SNPedia
UniProt Variants
Variants in Papers
Web Sequences
-   COVID-19
COVID GWAS v4
COVID GWAS v3
Rare Harmful Vars
-   mRNA and EST
CGAP SAGE
Gene Bounds
H-Inv
Human ESTs
Human mRNAs
Human RNA Editing
Other ESTs
Other mRNAs
Poly(A)
PolyA-Seq
SIB Alt-Splicing
Spliced ESTs
UniGene
-   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
ENCODE Regulation
CD34 DnaseI
CpG Islands
ENC Chromatin
ENC DNA Methyl
ENC DNase/FAIRE
ENC Histone
ENC RNA Binding
ENC TF Binding
FSU Repli-chip
GeneHancer
Genome Segments
GTEx Combined eQTL
GTEx Tissue eQTL
JASPAR Transcription Factors
NKI Nuc Lamina
ORegAnno
Rao 2014 Hi-C
ReMap ChIP-seq
Stanf Nucleosome
SUNY SwitchGear
SwitchGear TSS
TFBS Conserved
TS miRNA Targets
UCSF Brain Methyl
UMMS Brain Hist
UW Repli-seq
Vista Enhancers
-   Comparative Genomics
Conservation
Cons 46-Way
Cons Indels MmCf
Evo Cpg
GERP
phastBias gBGC
Primate Chain/Net
Placental Chain/Net
Vertebrate Chain/Net
CHM13 alignments
+   Neandertal Assembly and Analysis
+   Denisova Assembly and Analysis
-   Variation
dbSNP 155
1000G Archive
Array Probesets
dbSNP Archive
dbVar Common Struct Var
updated DGV Struct Var
EVS Variants
ExAC
Genome In a Bottle
Genome Variants
GIS DNA PET
gnomAD
HAIB Genotype
HapMap SNPs
HGDP Allele Freq
Platinum Genomes
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
NumtS Sequence
Segmental Dups
Self Chain
Simple Repeats
WM + SDust
Invisible link