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QUERY TYPE Select query type and 'AlleleID','GeneID','GeneSymbol' and 'HGNC_ID' QUERY ITEM Enter the AlleleID,GeneID,GeneSymbol or HGNC_ID PAM Select PAM type between 'NGG' and 'NG' DIRECTION Select edit direction which means to install or correct pathogenic human genetic variants ASSEMBLY HISTORY

Query Type Query Item PAM Direction Time
AlleleID 929884 NGG install 20230321025558
GeneID 148398 NGG install 20230321024624
AlleleID 929884 NGG install 20230321024118
AlleleID 929884 NGG install 20230321022957
AlleleID 929884 NGG install 20230321022205
AlleleID 929884 NGG install 20230210153746
AlleleID 526296 NGG install 20230210153321
AlleleID 526296 NGG install 20230206151102
AlleleID 929884 NGG install 20221130025927
AlleleID 929884 NGG install 20221130025918