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GRCh37/hg19 16q24.1(chr16:85602570-85775232)x3 AND See cases

Significance: Likely benign
ClinVar: RCV000447245

Variant: GRCh37/hg19 16q24.1(chr16:85602570-85775232)x3

Type: Variant
Allele: GRCh37/hg19 16q24.1(chr16:85602570-85775232)x3 382212
Gene:
Type: copy number gain
Location: Chr16: 85602570 - 85775232 - assembly GRCh37
References: dbVar: nsv2777163
dbVar: nssv13648142

Condition

PhenotypeInstruction: See cases