GENETIC ENCYCLOPEDIA
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NC_000011.9:g.(?_118007722)_(119170511_?)del AND Long QT syndrome 10

Significance: Uncertain significance
ClinVar: RCV000816632

Variant: NC_000011.9:g.(?_118007722)_(119170511_?)del

Type: Variant
Allele: NC_000011.9:g.(?_118007722)_(119170511_?)del 652157
Gene:
Type: Deletion
Location: Chr11: 118007722 - 119170511 - assembly GRCh37

Condition

Disease: Long QT syndrome 10