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GRCh37/hg19 7p14.1(chr7:40095110-40256612)x1 AND See cases

Significance: Likely benign
ClinVar: RCV000447190

Variant: GRCh37/hg19 7p14.1(chr7:40095110-40256612)x1

Type: Variant
Allele: GRCh37/hg19 7p14.1(chr7:40095110-40256612)x1 382590
Gene:
Type: copy number loss
Location: Chr7: 40095110 - 40256612 - assembly GRCh37
References: dbVar: nsv931442
dbVar: nssv1609410

Condition

PhenotypeInstruction: See cases