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Human Genome Region REGION216

Assembly:
GRCh38.p14
Location:
chr10:65,503,225-65,684,914
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KQ090020.1 NW_013171806.1 NOVEL Unavailable Unavailable Unavailable
           

REGION216 -- chr10 (CM000672.2):65,503,225-65,684,914