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Human Genome Region REGION136

Assembly:
GRCh38.p13
Location:
chr5:33,800,665-33,963,236
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270794.1 NT_187551.1 ALT 164,558 122 2,079
           

REGION136 -- chr5 (NC_000005.10):33,800,665-33,963,236