GENETIC ENCYCLOPEDIA
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GRCh37/hg19 22q13.1(chr22:40794180-40794596)x0 AND not provided

Significance: Benign
ClinVar: RCV000741983

Variant: GRCh37/hg19 22q13.1(chr22:40794180-40794596)x0

Type: Variant
Allele: GRCh37/hg19 22q13.1(chr22:40794180-40794596)x0 596683
Gene:
Type: copy number loss
Location: Chr22: 40794180 - 40794596 - assembly GRCh37

Condition

Disease: not provided