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Human Genome Region REGION146

Assembly:
GRCh38.p14
Location:
chr7:76,500,982-76,722,751
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270809.1 NT_187561.1 ALT Unavailable Unavailable Unavailable
           

REGION146 -- chr7 (CM000669.2):76,500,982-76,722,751