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Human Genome Region REGION137

Assembly:
GRCh38.p14
Location:
chr5:125,279,466-125,444,151
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270796.1 NT_187549.1 ALT Unavailable Unavailable Unavailable
           

REGION137 -- chr5 (CM000667.2):125,279,466-125,444,151