ClinVar

GRCh37/hg19 15q11.2(chr15:22770422-24058623)x3

Genes:

• MAGEL2:MAGE family member L2 [Gene - OMIM - HGNC]
• NIPA1:NIPA magnesium transporter 1 [Gene - OMIM - HGNC]
• NIPA2:NIPA magnesium transporter 2 [Gene - OMIM - HGNC]
• CYFIP1:cytoplasmic FMR1 interacting protein 1 [Gene - OMIM - HGNC]
• GOLGA6L2:golgin A6 family like 2 [Gene - HGNC]
• MKRN3:makorin ring finger protein 3 [Gene - OMIM - HGNC]
• NDN:necdin, MAGE family member [Gene - OMIM - HGNC]
• TUBGCP5:tubulin gamma complex associated protein 5 [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

15q11.2

Genomic location:

Chr15: 22770422 - 24058623 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 15q11.2(chr15:22770422-24058623)x3

HGVS:

This HGVS expression did not pass validation