Human hg38 chr17:7,668,421-7,687,490 UCSC Genome Browser v474

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UCSC Genome Browser on Human (GRCh38/hg38)
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chr17:7,668,421-7,687,490 19,070 bp.

Hub: Variant Effect Maps

No Info

AID 00000106-a-1

AID 00000106-b-1

AID 00000106-c-1

ALDOB 00000006-a-1

alpha-synuclein 00000045-a-1

alpha-synuclein 00000045-b-1

alpha-synuclein 00000045-c-1

alpha-synuclein 00000045-d-1

alpha-synuclein 00000045-e-1

alpha-synuclein 00000045-f-1

alpha-synuclein 00000045-g-1

alpha-synuclein 00000045-h-1

alpha-synuclein 00000045-i-1

alpha-synuclein 00000045-j-1

alpha-synuclein 00000045-k-1

alpha-synuclein 00000045-l-1

BCL11A 00000014-a-1

BRAF 00000091-a-1

BRCA1 00000093-a-1

BRCA1 00000097-0-1

BRCA1 00000097-a-1

BRCA1 00000097-b-1

BRCA1 00000097-c-1

BRCA1 00000097-d-1

BRCA1 00000097-e-1

BRCA1 00000097-f-1

BRCA1 00000097-g-1

BRCA1 00000097-h-1

BRCA1 00000097-i-1

BRCA1 00000097-j-1

BRCA1 00000097-k-1

BRCA1 00000097-l-1

BRCA1 00000097-m-1

BRCA1 00000097-n-1

BRCA1 00000097-o-1

BRCA1 00000097-p-1

BRCA1 00000097-q-1

BRCA1 00000097-r-1

BRCA1 00000097-s-1

BRCA1 00000097-t-1

BRCA1 00000097-u-1

BRCA1 00000097-v-1

BRCA1 00000097-w-1

BRCA1 00000097-x-1

BRCA1 00000097-y-1

BRCA1 00000097-z-1

CCR5 00000047-a-1

CCR5 00000047-b-1

CCR5 00000047-c-1

CXCR4 00000048-a-1

CXCR4 00000048-b-1

CXCR4 00000048-c-1

CYP2C19 00000062-b-1

CYP2C9 00000062-a-1

CYP2C9 00000095-a-1

CYP2C9 00000095-b-1

ECR11 00000007-a-1

ErbB2 00000051-b-1

F9 00000015-a-1

FOXE1 00000016-a-1

GCK 00000096-a-1

GDI1 00000066-a-1

Glycophorin 00000051-c-1

GP1BB 00000017-a-1

HBB 00000018-a-1

HBG1 00000019-a-1

HNF4A 00000020-a-1

IRF4 00000021-a-1

IRF6 00000022-a-1

MAPK1 00000103-a-1

MAPK1 00000103-b-1

MAPK1 00000103-c-1

MAPK1 00000103-d-1

Minigene 00000083-a-1

Minigene 00000083-b-1

Minigene 00000083-c-1

Minigene 00000083-d-1

Minigene 00000083-e-1

Minigene 00000083-f-1

Minigene 00000083-g-1

Minigene 00000083-h-1

Minigene 00000083-i-1

Minigene 00000083-j-1

MSH2 00000050-a-1

MSMB 00000024-a-1

MYC 00000025-a-1

MYC 00000026-a-1

NCS1 00000065-a-1

NUDT15 00000055-0-1

NUDT15 00000055-a-1

NUDT15 00000055-b-1

PKLR 00000027-a-1

PKLR 00000027-b-1

PSAT1 00000107-a-1

PTEN 00000013-a-1

PTEN 00000101-a-1

PTEN 00000102-0-1

RAF 00000061-a-1

RAF 00000061-b-1

RAF 00000061-c-1

RAF 00000061-d-1

RAF 00000061-e-1

RAF 00000061-f-1

RAF 00000061-g-1

RAF 00000061-h-1

RAF 00000061-i-1

Ras 00000057-a-1

Ras 00000057-b-1

Ras 00000057-c-1

RET 00000028-a-1

RHO 00000099-a-1

SCN5A 00000098-a-1

SORT1 00000029-b-1

Src 00000041-a-1

Src 00000041-b-1

TCF7L2 00000030-a-1

TECR 00000067-a-1

TERT 00000031-a-1

TERT 00000031-b-1

TERT 00000031-c-1

TERT 00000031-d-1

TP53 00000068-a-1

TP53 00000068-b-1

TP53 00000068-c-1

TPMT 00000013-b-1

UC88 00000032-a-1

VKOR 00000078-a-1

VKOR 00000078-b-1

ZFAND3 00000033-a-1

ZRS 00000034-a-1

ZRS 00000034-b-1

Hub: Variant Effect Maps

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Mapping and Sequencing

p14 Fix Patches

p14 Alt Haplotypes

Assembly Tracks

Chromosome Band

Exome Probesets

LiftOver & ReMap

updated Problematic Regions

Genes and Gene Predictions

updated GENCODE V47

GENCODE Archive

updated GENCODE Versions

IKMC Genes Mapped

LRG Transcripts

MGC/ORFeome Genes

Pfam in GENCODE

Prediction Archive

UCSC Alt Events

Phenotype and Literature

AbSplice Scores

Cancer Gene Expr

ClinVar Variants

Constraint scores

Development Delay

Dosage Sensitivity

Gene Interactions

TCGA Pan-Cancer

UniProt Variants

Variants in Papers

Human Pangenome - HPRC

Multiple Alignment

Pairwise Alignments

mRNA and EST

SIB Alt-Splicing

Expression

GTEx RNA-Seq Coverage

EPDnew Promoters

GTEx Transcript

GWIPS-viz Riboseq

miRNA Tissue Atlas

Single Cell Expression

Single Cell RNA-seq

Blood (PBMC) Hao

Cortex Velmeshev

Cross Tissue Nuclei

Fetal Gene Atlas

Heart Cell Atlas

Liver MacParland

Lung Travaglini

Muscle De Micheli

Placenta Vento-Tormo

Skin Sole-Boldo

Regulation

ENCODE Regulation

Hi-C and Micro-C

JASPAR Transcription Factors

RefSeq Func Elems

VISTA Enhancers

Comparative Genomics

Cons 30 Primates

Primate Chain/Net

Placental Chain/Net

Vertebrate Chain/Net

CHM13 alignments

Variation

Array Probesets

dbVar Common Struct Var

Genome In a Bottle

new gnomAD Variants

Platinum Genomes

Repeats

Interrupted Rpts

RepeatMasker Viz.