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GRCh38/hg38 22q13.2(chr22:40769910-41360090)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000134514

Variant: GRCh38/hg38 22q13.2(chr22:40769910-41360090)x3

Type: Variant
Allele: GRCh38/hg38 22q13.2(chr22:40769910-41360090)x3 154863
Gene:
Type: copy number gain
Location: Chr22: 39495860 - 40086040 - assembly NCBI36
Chr22: 40769910 - 41360090 - assembly GRCh38
Chr22: 41165914 - 41756094 - assembly GRCh37
Chr22: 40769910 - 41360090 - assembly GRCh38
References: dbVar: nsv497600
dbVar: nssv583687

Condition

PhenotypeInstruction: See cases