The UMD Central
Deletions analysis

This option is used to check if a repeated sequence could be involved in the mutational event. The repeated sequences is usually localized at each extremity of the deletion. This situation if found habitually when a deletion involving more than 2 nt is present. When the deletion involves only 1 nt, it is mostly localized in a stretch of this nucleotide (polyC for example).

Choose UMD databases to use for this analysis:

APC ATP7B BRCA1 BRCA2 CDH23 CFTR
COL3A1 CSA CSB DFNB1-GJB2 DMD DNM2
DPYD DYSF EMD F7 FBN1 FBN2
LDLR LMNA MEN1 MLH1 MSH2 MSH6
MYO7A PCDH15 PTCH1 SMN1 TGFBR1 TGFBR2
THAP1 TP53 USH1C USH1G USH2A USH3A
VHL