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GRCh37/hg19 2q23.1(chr2:148957572-149100105)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000446610

Variant: GRCh37/hg19 2q23.1(chr2:148957572-149100105)x1

Type: Variant
Allele: GRCh37/hg19 2q23.1(chr2:148957572-149100105)x1 381387
Gene:
Type: copy number loss
Location: Chr2: 148957572 - 149100105 - assembly GRCh37
References: dbVar: nsv2772647
dbVar: nssv13641436

Condition

PhenotypeInstruction: See cases