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GRCh37/hg19 4q32.2(chr4:162610999-162866608)x1 AND See cases

Significance: Likely benign
ClinVar: RCV000446591

Variant: GRCh37/hg19 4q32.2(chr4:162610999-162866608)x1

Type: Variant
Allele: GRCh37/hg19 4q32.2(chr4:162610999-162866608)x1 383989
Gene:
Type: copy number loss
Location: Chr4: 162610999 - 162866608 - assembly GRCh37
References: dbVar: nsv2777015
dbVar: nssv13652225

Condition

PhenotypeInstruction: See cases