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GRCh38/hg38 15q21.3-22.2(chr15:57456076-61907285)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000050884

Variant: GRCh38/hg38 15q21.3-22.2(chr15:57456076-61907285)x1

Type: Variant
Allele: GRCh38/hg38 15q21.3-22.2(chr15:57456076-61907285)x1 71815
Gene:
Type: copy number loss
Location: Chr15: 57748274 - 62199484 - assembly GRCh37
Chr15: 55535566 - 59986776 - assembly NCBI36
Chr15: 57456076 - 61907285 - assembly GRCh38
Chr15: 57456076 - 61907285 - assembly GRCh38
References: dbVar: nsv529463
dbVar: nssv577506

Condition

PhenotypeInstruction: See cases