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GRCh38/hg38 22q13.2(chr22:40860894-41306006)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000050897

Variant: GRCh38/hg38 22q13.2(chr22:40860894-41306006)x3

Type: Variant
Allele: GRCh38/hg38 22q13.2(chr22:40860894-41306006)x3 71828
Gene:
Type: copy number gain
Location: Chr22: 39586844 - 40031956 - assembly NCBI36
Chr22: 40860894 - 41306006 - assembly GRCh38
Chr22: 41256898 - 41702010 - assembly GRCh37
Chr22: 40860894 - 41306006 - assembly GRCh38
References: dbVar: nsv529476
dbVar: nssv581078
dbVar: nssv581077

Condition

PhenotypeInstruction: See cases