GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3 |
copy number gain |
See cases [RCV000050635] |
Chr19:17176767..34924150 [GRCh38] Chr19:17287576..35415054 [GRCh37] Chr19:17148576..40106894 [NCBI36] Chr19:19p13.11-q13.11 |
pathogenic |
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3 |
copy number gain |
See cases [RCV000052912] |
Chr19:13974677..27839676 [GRCh38] Chr19:14085489..28330584 [GRCh37] Chr19:13946489..33022424 [NCBI36] Chr19:19p13.12-q11 |
pathogenic |
GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3 |
copy number gain |
See cases [RCV000136696] |
Chr19:15133594..24193591 [GRCh38] Chr19:15244405..24376393 [GRCh37] Chr19:15105405..24168233 [NCBI36] Chr19:19p13.12-12 |
pathogenic|likely pathogenic |
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 |
copy number gain |
See cases [RCV000133888] |
Chr19:11227942..44626354 [GRCh38] Chr19:11338618..45129651 [GRCh37] Chr19:11199618..49821491 [NCBI36] Chr19:19p13.2-q13.31 |
pathogenic |
GRCh38/hg38 19p12(chr19:22987611-23189484)x1 |
copy number loss |
See cases [RCV000140874] |
Chr19:22987611..23189484 [GRCh38] Chr19:23170413..23372286 [GRCh37] Chr19:22962253..23164126 [NCBI36] Chr19:19p12 |
uncertain significance |
GRCh37/hg19 19p12(chr19:22867705-23645194)x4 |
copy number gain |
See cases [RCV000598637] |
Chr19:22867705..23645194 [GRCh37] Chr19:19p12 |
uncertain significance |
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 |
copy number gain |
See cases [RCV000511289] |
Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic|uncertain significance |
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) |
copy number gain |
See cases [RCV000512296] |
Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic |
chr19:19230868-24115369 complex variant |
complex |
Breast ductal adenocarcinoma [RCV000207223] |
Chr19:19230868..24115369 [GRCh37] Chr19:19p13.11-12 |
uncertain significance |
GRCh37/hg19 19p13.11-11(chr19:16526787-24631604)x3 |
copy number gain |
not provided [RCV000752593] |
Chr19:16526787..24631604 [GRCh37] Chr19:19p13.11-11 |
pathogenic |
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 |
copy number gain |
not provided [RCV000752439] |
Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic |
GRCh37/hg19 19p12(chr19:23262262-23379015)x1 |
copy number loss |
not provided [RCV001007039] |
Chr19:23262262..23379015 [GRCh37] Chr19:19p12 |
likely benign |
GRCh37/hg19 19p12(chr19:23217767-23956831)x3 |
copy number gain |
not provided [RCV002473524] |
Chr19:23217767..23956831 [GRCh37] Chr19:19p12 |
uncertain significance |
GRCh37/hg19 19p12-11(chr19:22635439-24505637)x3 |
copy number gain |
not provided [RCV000684090] |
Chr19:22635439..24505637 [GRCh37] Chr19:19p12-11 |
likely benign |
GRCh37/hg19 19p12(chr19:22789865-23338320)x3 |
copy number gain |
not provided [RCV000684083] |
Chr19:22789865..23338320 [GRCh37] Chr19:19p12 |
likely benign |
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 |
copy number gain |
not provided [RCV000752444] |
Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic |
GRCh37/hg19 19p12(chr19:23030170-23316525)x1 |
copy number loss |
not provided [RCV001259367] |
Chr19:23030170..23316525 [GRCh37] Chr19:19p12 |
likely benign |
GRCh37/hg19 19p12-11(chr19:22630650-24487350)x3 |
copy number gain |
See cases [RCV001007435] |
Chr19:22630650..24487350 [GRCh37] Chr19:19p12-11 |
uncertain significance |
GRCh37/hg19 19p12(chr19:23166550-23307438)x1 |
copy number loss |
not provided [RCV001259368] |
Chr19:23166550..23307438 [GRCh37] Chr19:19p12 |
likely benign |
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3 |
copy number gain |
Specific learning disability [RCV001801194] |
Chr19:19546923..41313229 [GRCh37] Chr19:19p13.11-q13.2 |
pathogenic |
NM_001277403.2(ZNF730):c.906dup (p.Lys303Ter) |
duplication |
not provided [RCV003425080] |
Chr19:23145949..23145950 [GRCh38] Chr19:23328751..23328752 [GRCh37] Chr19:19p12 |
likely benign |
GRCh37/hg19 19p12-q12(chr19:22521477-28934362)x3 |
copy number gain |
not provided [RCV004819643] |
Chr19:22521477..28934362 [GRCh37] Chr19:19p12-q12 |
uncertain significance |