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GRCh37/hg19 22q13.1-13.2(chr22:40233644-41655673)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000448955

Variant: GRCh37/hg19 22q13.1-13.2(chr22:40233644-41655673)x3

Type: Variant
Allele: GRCh37/hg19 22q13.1-13.2(chr22:40233644-41655673)x3 383407
Gene:
Type: copy number gain
Location: Chr22: 40233644 - 41655673 - assembly GRCh37
References: dbVar: nsv2773300
dbVar: nssv13656085

Condition

PhenotypeInstruction: See cases