GENETIC ENCYCLOPEDIA
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GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 AND not provided

Significance: Pathogenic
ClinVar: RCV000752439

Variant: GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3

Type: Variant
Allele: GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 607139
Gene:
Type: copy number gain
Location: Chr19: 68029 - 59110290 - assembly GRCh37

Condition

Disease: not provided