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GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000051622

Variant: GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1

Type: Variant
Allele: GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1 72477
Gene:
Type: copy number loss
Location: Chr15: 57860148 - 63311614 - assembly GRCh37
Chr15: 55647440 - 61098667 - assembly NCBI36
Chr15: 57567950 - 63019415 - assembly GRCh38
Chr15: 57567950 - 63019415 - assembly GRCh38
References: dbVar: nsv530145
dbVar: nssv577507

Condition

PhenotypeInstruction: See cases