GENETIC ENCYCLOPEDIA
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GRCh37/hg19 6q13(chr6:74341681-74351732)x3 AND See cases

Significance: Likely benign
ClinVar: RCV000447221

Variant: GRCh37/hg19 6q13(chr6:74341681-74351732)x3

Type: Variant
Allele: GRCh37/hg19 6q13(chr6:74341681-74351732)x3 381883
Gene:
Type: copy number gain
Location: Chr6: 74341681 - 74351732 - assembly GRCh37
References: dbVar: nsv2775383
dbVar: nssv13655667

Condition

PhenotypeInstruction: See cases