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Human Genome Region REGION171

Assembly:
GRCh38.p14
Location:
chr14:105,533,003-106,860,219
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270846.1 NT_187600.1 ALT Unavailable Unavailable Unavailable
           

REGION171 -- chr14 (CM000676.2):105,533,003-106,860,219