GENETIC ENCYCLOPEDIA
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NC_000022.10:g.(?_41264983)_(41729217_?)dup AND Nephronophthisis-like nephropathy 1

Significance: Uncertain significance
ClinVar: RCV000556646

Variant: NC_000022.10:g.(?_41264983)_(41729217_?)dup

Type: Variant
Allele: NC_000022.10:g.(?_41264983)_(41729217_?)dup 469864
Gene:
Type: Duplication
Location: Chr22: 40868979 - 41333213 - assembly GRCh38
Chr22: 41264983 - 41729217 - assembly GRCh37
Chr22: 40868979 - 41333213 - assembly GRCh38

Condition

Disease: Nephronophthisis-like nephropathy 1