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Homo sapiens

(human)
Assembly:

Assembly: GRCh38.p14

(GCF_000001405.40)
Search assembly
Examples
  • chr1:1,500,000-2,000,000
  • chr2: 1.5M - 2M
  • chr2: 1.5M-2,540.2K
  • 2:1,500,000-2,000,000
  • 3: 21.33M - 22.01M
  • 3: 21.335M..21.337M
  • chr1:1,500,000 / 200
  • chr1:101,500,200
  • 1:101,500,200
  • 1:1,500K/0.5K

Pick Assembly

Select an assembly and annotation to change view

Tracks and User Data

Name Location

Supported File/Data types

  • Uploaded tracks
    • BED
    • GFF3
    • GTF
    • GVF
    • VCF
    • HGVS
    • WIG
    • ASN.1 (text and binary)
  • Remote tracks
    • Remote BAM.bai or CSI index file present at same location
    • Remote VCFun-indexed up to 2000 lines or with an index file present at the same location
    • BigBed
    • BigWig

History

Select gene from history

Assembly Region Details

Features of Interest
Other sequence representations
for assembly region(s) in view- none -- loading …
Sequence IDType
Back to region
No GRC genome issues in rangeAdd Track
Not applicable for this organism/assembly
 Collapse sidebar [NC_000009.12:91,070,805 - 91,071,892
Region Gene
Transcript
Exons: click an exon to zoom in, mouse over to see details
No exons
LINC02957 Exon Navigator: There are no genes in the region LINC02937

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Source database
In ClinVar
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1000 Genomes MAF
GO_ESP MAF
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Has publications
Variant ID Location Variant type Gene Molecular consequences Most severe clinical significance Alleles 1000G MAF GO-ESP MAF ExAC MAF Publications
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