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GRCh37/hg19 15q24.2(chr15:75562397-75580623)x3 AND See cases

Significance: Benign
ClinVar: RCV000446608

Variant: GRCh37/hg19 15q24.2(chr15:75562397-75580623)x3

Type: Variant
Allele: GRCh37/hg19 15q24.2(chr15:75562397-75580623)x3 380995
Gene:
Type: copy number gain
Location: Chr15: 75562397 - 75580623 - assembly GRCh37
References: dbVar: nsv2770600
dbVar: nssv13655837
dbVar: nssv13649798

Condition

PhenotypeInstruction: See cases