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GRCh37/hg19 17p13.3(chr17:6160-1114083)x1 AND See cases

Significance: Uncertain significance
ClinVar: RCV000446658

Variant: GRCh37/hg19 17p13.3(chr17:6160-1114083)x1

Type: Variant
Allele: GRCh37/hg19 17p13.3(chr17:6160-1114083)x1 380918
Gene:
Type: copy number loss
Location: Chr17: 6160 - 1114083 - assembly GRCh37
References: dbVar: nsv2770191
dbVar: nssv13641654

Condition

PhenotypeInstruction: See cases