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GRCh37/hg19 2q37.1(chr2:233055165-233763272)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447269

Variant: GRCh37/hg19 2q37.1(chr2:233055165-233763272)x3

Type: Variant
Allele: GRCh37/hg19 2q37.1(chr2:233055165-233763272)x3 380609
Gene:
Type: copy number gain
Location: Chr2: 233055165 - 233763272 - assembly GRCh37
References: dbVar: nsv2768264
dbVar: nssv13654013

Condition

PhenotypeInstruction: See cases