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Items: 1 to 100 of 395

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr11:65508902-67473140
GRCh38:
Chr11:65741431-67705669
See casesPathogenic
(Oct 24, 2012)
no assertion criteria providedVCV000154814
2.
GRCh37:
Chr11:65960973-67658241
GRCh38:
Chr11:66193502-67890770
See casesPathogenic
(Aug 12, 2011)
criteria provided, single submitterVCV000059757
3.
GRCh37:
Chr11:66653381-67465721
GRCh38:
Chr11:66885910-67698250
See casesPathogenic
(Aug 12, 2011)
criteria provided, single submitterVCV000058892
4.
GRCh37:
Chr11:66984735-69263366
GRCh38:
Chr11:67217264-69448598
See casesLikely pathogenic
(Aug 5, 2011)
no assertion criteria providedVCV000146304
5.
GRCh37:
Chr11:67164667-67411909
GRCh38:
Chr11:67397196-67644438
See casesBenign
(Jan 30, 2010)
no assertion criteria providedVCV000147720
6.
GRCh37:
Chr11:67213624-68446541
GRCh38:
Chr11:67446153-68679073
See casesPathogenic
(Aug 12, 2011)
criteria provided, single submitterVCV000058893
7.
GRCh37:
Chr11:67249418-67255234
GRCh38:
Chr11:67481947-67487763
AIPSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041158
8.
GRCh37:
Chr11:67250230-67250231
GRCh38:
Chr11:67482759-67482760
AIPnot providedBenign
(Aug 19, 2019)
criteria provided, single submitterVCV001234779
9.
GRCh37:
Chr11:67250360-67250361
GRCh38:
Chr11:67482889-67482890
AIPno interpretation for the single variantno interpretation for the single variantVCV000424703
10.
GRCh37:
Chr11:67250410
GRCh38:
Chr11:67482939
AIPno interpretation for the single variantno interpretation for the single variantVCV000242676
11.
GRCh37:
Chr11:67250545
GRCh38:
Chr11:67483074
AIPSomatotroph adenomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000879697
12.
GRCh37:
Chr11:67250546
GRCh38:
Chr11:67483075
AIPSomatotroph adenomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000305719
13.
GRCh37:
Chr11:67250607
GRCh38:
Chr11:67483136
AIPSomatotroph adenomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000305720
14.
GRCh37:
Chr11:67250618
GRCh38:
Chr11:67483147
AIPSomatotroph adenomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000305721
15.
GRCh37:
Chr11:67250625
GRCh38:
Chr11:67483154
AIPSomatotroph adenomaLikely benign
(Jun 21, 2012)
no assertion criteria providedVCV000041159
16.
GRCh37:
Chr11:67250627
GRCh38:
Chr11:67483156
AIPHereditary cancer-predisposing syndromeUncertain significance
(Nov 19, 2019)
criteria provided, single submitterVCV000824477
17.
GRCh37:
Chr11:67250628
GRCh38:
Chr11:67483157
AIPSomatotroph adenomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000305722
18.
GRCh37:
Chr11:67250631
GRCh38:
Chr11:67483160
AIPM1TSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041173
19.
GRCh37:
Chr11:67250632
GRCh38:
Chr11:67483161
AIPM1IPituitary adenoma, familial isolatedLikely pathogenic
(Aug 19, 2016)
criteria provided, single submitterVCV000253315
20.
GRCh37:
Chr11:67250632-67250633
GRCh38:
Chr11:67483161-67483162
AIPA2fsSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041177
21.
GRCh37:
Chr11:67250633
GRCh38:
Chr11:67483162
AIPA2PHereditary cancer-predisposing syndromeUncertain significance
(May 8, 2019)
criteria provided, single submitterVCV000825361
22.
GRCh37:
Chr11:67250639
GRCh38:
Chr11:67483168
AIPI4Fnot providedUncertain significance
(Mar 27, 2020)
criteria provided, single submitterVCV001020574
23.
GRCh37:
Chr11:67250641
GRCh38:
Chr11:67483170
AIPnot providedLikely benign
(Nov 26, 2019)
criteria provided, single submitterVCV001154113
24.
GRCh37:
Chr11:67250641
GRCh38:
Chr11:67483170
AIPI4MHereditary cancer-predisposing syndrome, not providedUncertain significance
(Aug 30, 2020)
criteria provided, multiple submitters, no conflictsVCV000818845
25.
GRCh37:
Chr11:67250652
GRCh38:
Chr11:67483181
AIPL8Rnot providedUncertain significance
(Aug 10, 2020)
criteria provided, single submitterVCV001047798
26.
GRCh37:
Chr11:67250653
GRCh38:
Chr11:67483182
AIPnot providedLikely benign
(Jul 21, 2020)
criteria provided, single submitterVCV001078174
27.
GRCh37:
Chr11:67250654
GRCh38:
Chr11:67483183
AIPR9Wnot providedUncertain significance
(Jul 1, 2020)
criteria provided, multiple submitters, no conflictsVCV000388468
28.
GRCh37:
Chr11:67250655
GRCh38:
Chr11:67483184
AIPR9QAcroleukopathy, symmetric, Pituitary dependent hypercortisolism, Somatotroph adenoma,
not provided, Somatotroph adenoma, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Nov 3, 2021)
criteria provided, conflicting interpretationsVCV000485052
29.
GRCh37:
Chr11:67250665
GRCh38:
Chr11:67483194
AIPnot providedLikely benign
(Jun 16, 2020)
criteria provided, single submitterVCV001102270
30.
GRCh37:
Chr11:67250665
GRCh38:
Chr11:67483194
AIPHereditary cancer-predisposing syndrome, not provided, Somatotroph adenoma
Benign/Likely benign
(Dec 1, 2020)
criteria provided, multiple submitters, no conflictsVCV000305723
31.
GRCh37:
Chr11:67250669
GRCh38:
Chr11:67483198
AIPQ14*Hereditary cancer-predisposing syndrome, Somatotroph adenoma, Pituitary adenoma predisposition
Pathogenic
(Sep 25, 2019)
criteria provided, single submitterVCV000004886
32.
GRCh37:
Chr11:67250670
GRCh38:
Chr11:67483199
AIPQ14PHereditary cancer-predisposing syndrome, not providedUncertain significance
(Oct 27, 2020)
criteria provided, multiple submitters, no conflictsVCV000824668
33.
GRCh37:
Chr11:67250676
GRCh38:
Chr11:67483205
AIPR16HPituitary adenoma, familial isolated, Somatotroph adenoma, Hereditary cancer-predisposing syndrome,
not provided
Conflicting interpretations of pathogenicity
(Nov 3, 2021)
criteria provided, conflicting interpretationsVCV000041184
34.
GRCh37:
Chr11:67250682
GRCh38:
Chr11:67483211
AIPI18THereditary cancer-predisposing syndromeUncertain significance
(Dec 20, 2017)
criteria provided, single submitterVCV000825703
35.
GRCh37:
Chr11:67250686
GRCh38:
Chr11:67483215
AIPnot providedLikely benign
(Dec 26, 2019)
criteria provided, single submitterVCV001083285
36.
GRCh37:
Chr11:67250691
GRCh38:
Chr11:67483220
AIPG21Anot providedUncertain significance
(Jun 23, 2020)
criteria provided, single submitterVCV000963750
37.
GRCh37:
Chr11:67250692
GRCh38:
Chr11:67483221
AIPnot providedLikely benign
(Oct 23, 2019)
criteria provided, single submitterVCV001128637
38.
GRCh37:
Chr11:67250693
GRCh38:
Chr11:67483222
AIPR22*Somatotroph adenomaPathogenic/Likely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000004894
39.
GRCh37:
Chr11:67250695-67250700
GRCh38:
Chr11:67483224-67483229
AIPSomatotroph adenomaPathogenic/Likely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000004889
40.
GRCh37:
Chr11:67250697
GRCh38:
Chr11:67483226
AIPG23ESomatotroph adenoma, Hereditary cancer-predisposing syndrome, not provided
Benign/Likely benign
(Nov 28, 2020)
criteria provided, multiple submitters, no conflictsVCV000305724
41.
GRCh37:
Chr11:67250699
GRCh38:
Chr11:67483228
AIPE24Qnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Aug 6, 2020)
criteria provided, multiple submitters, no conflictsVCV000826838
42.
GRCh37:
Chr11:67250699
GRCh38:
Chr11:67483228
AIPE24*Somatotroph adenoma, not providedPathogenic
(Mar 12, 2020)
criteria provided, single submitterVCV000041196
43.
GRCh37:
Chr11:67250701
GRCh38:
Chr11:67483230
AIPE24Dnot provided, Hereditary cancer-predisposing syndromeConflicting interpretations of pathogenicity
(Nov 15, 2020)
criteria provided, conflicting interpretationsVCV000485057
44.
GRCh37:
Chr11:67250702
GRCh38:
Chr11:67483231
AIPL25Fnot providedUncertain significance
(Aug 14, 2019)
criteria provided, single submitterVCV000954536
45.
GRCh37:
Chr11:67250703-67250710
GRCh38:
Chr11:67483232-67483239
AIPSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041203
46.
GRCh37:
Chr11:67250708
GRCh38:
Chr11:67483237
AIPD27Hnot providedUncertain significance
(Sep 3, 2020)
criteria provided, single submitterVCV001063510
47.
GRCh37:
Chr11:67250713
GRCh38:
Chr11:67483242
AIPnot providedLikely benign
(Jun 29, 2020)
criteria provided, single submitterVCV001110711
48.
GRCh37:
Chr11:67250714
GRCh38:
Chr11:67483243
AIPQ29*not providedPathogenic
(Jul 30, 2019)
criteria provided, single submitterVCV000958713
49.
GRCh37:
Chr11:67250717
GRCh38:
Chr11:67483246
AIPD30Ynot providedUncertain significance
(Sep 8, 2019)
criteria provided, single submitterVCV000954484
50.
GRCh37:
Chr11:67250719
GRCh38:
Chr11:67483248
AIPnot providedLikely benign
(Aug 20, 2020)
criteria provided, single submitterVCV001117434
51.
GRCh37:
Chr11:67250722
GRCh38:
Chr11:67483251
AIPnot providedUncertain significance
(Jun 8, 2020)
criteria provided, single submitterVCV000864069
52.
GRCh37:
Chr11:67250722
GRCh38:
Chr11:67483251
AIPHereditary cancer-predisposing syndromeLikely benign
(May 18, 2017)
criteria provided, single submitterVCV000485068
53.
GRCh37:
Chr11:67250726
GRCh38:
Chr11:67483255
AIPK33Enot providedUncertain significance
(Dec 30, 2019)
criteria provided, single submitterVCV000859012
54.
GRCh37:
Chr11:67250736
GRCh38:
Chr11:67483265
AIPnot providedLikely benign
(Dec 3, 2020)
criteria provided, single submitterVCV001121478
55.
GRCh37:
Chr11:67250738
GRCh38:
Chr11:67483267
AIPnot providedLikely benign
(Nov 27, 2019)
criteria provided, single submitterVCV001083668
56.
GRCh37:
Chr11:67253423-67254984
GRCh38:
Chr11:67485952-67487513
AIPSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041161
57.
GRCh37:
Chr11:67254459
GRCh38:
Chr11:67486988
AIPnot providedConflicting interpretations of pathogenicity
(Jan 11, 2021)
criteria provided, conflicting interpretationsVCV000596138
58.
GRCh37:
Chr11:67254470
GRCh38:
Chr11:67486999
AIPnot providedLikely benign
(Sep 8, 2020)
criteria provided, single submitterVCV001153003
59.
GRCh37:
Chr11:67254471
GRCh38:
Chr11:67487000
AIPnot providedBenign
(Nov 18, 2020)
criteria provided, single submitterVCV001169842
60.
GRCh37:
Chr11:67254477
GRCh38:
Chr11:67487006
AIPA34SHereditary cancer-predisposing syndromeUncertain significance
(Jul 19, 2019)
criteria provided, single submitterVCV000822003
61.
GRCh37:
Chr11:67254477
GRCh38:
Chr11:67487006
AIPA34THereditary cancer-predisposing syndromeUncertain significance
(Apr 19, 2018)
criteria provided, single submitterVCV000822001
62.
GRCh37:
Chr11:67254479
GRCh38:
Chr11:67487008
AIPSomatotroph adenomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000305725
63.
GRCh37:
Chr11:67254481
GRCh38:
Chr11:67487010
AIPT35Mnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Oct 6, 2020)
criteria provided, multiple submitters, no conflictsVCV000485058
64.
GRCh37:
Chr11:67254482
GRCh38:
Chr11:67487011
AIPHereditary cancer-predisposing syndrome, not providedLikely benign
(Sep 2, 2020)
criteria provided, multiple submitters, no conflictsVCV000818316
65.
GRCh37:
Chr11:67254485
GRCh38:
Chr11:67487014
AIPHereditary cancer-predisposing syndromeLikely benign
(Apr 25, 2018)
criteria provided, single submitterVCV000822137
66.
GRCh37:
Chr11:67254492
GRCh38:
Chr11:67487021
AIPR39Gnot providedUncertain significance
(Mar 5, 2020)
criteria provided, single submitterVCV001001466
67.
GRCh37:
Chr11:67254492
GRCh38:
Chr11:67487021
AIPR39Wnot providedUncertain significance
(Oct 5, 2020)
criteria provided, single submitterVCV000861039
68.
GRCh37:
Chr11:67254493
GRCh38:
Chr11:67487022
AIPR39Qnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Oct 4, 2019)
criteria provided, multiple submitters, no conflictsVCV000818481
69.
GRCh37:
Chr11:67254496
GRCh38:
Chr11:67487025
AIPT40MHereditary cancer-predisposing syndrome, not providedUncertain significance
(Jun 10, 2020)
criteria provided, multiple submitters, no conflictsVCV000818567
70.
GRCh37:
Chr11:67254497
GRCh38:
Chr11:67487026
AIPHereditary cancer-predisposing syndrome, not providedLikely benign
(Aug 14, 2020)
criteria provided, multiple submitters, no conflictsVCV000818603
71.
GRCh37:
Chr11:67254503
GRCh38:
Chr11:67487032
AIPnot providedLikely benign
(Feb 17, 2020)
criteria provided, single submitterVCV001127735
72.
GRCh37:
Chr11:67254509
GRCh38:
Chr11:67487038
AIPHereditary cancer-predisposing syndrome, Somatotroph adenoma, not specified,
not provided
Benign
(Dec 4, 2020)
criteria provided, multiple submitters, no conflictsVCV000259204
73.
GRCh37:
Chr11:67254510
GRCh38:
Chr11:67487039
AIPD45Nnot providedUncertain significance
(Aug 14, 2020)
criteria provided, single submitterVCV001040600
74.
GRCh37:
Chr11:67254512
GRCh38:
Chr11:67487041
AIPSomatotroph adenoma, Hereditary cancer-predisposing syndrome, not provided
Likely benign
(Nov 23, 2020)
criteria provided, multiple submitters, no conflictsVCV000041162
75.
GRCh37:
Chr11:67254513
GRCh38:
Chr11:67487042
AIPE46KHereditary cancer-predisposing syndromeUncertain significance
(Sep 6, 2019)
criteria provided, single submitterVCV000819007
76.
GRCh37:
Chr11:67254515-67254538
GRCh38:
Chr11:67487044-67487067
AIPSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041163
77.
GRCh37:
Chr11:67254516
GRCh38:
Chr11:67487045
AIPG47SHereditary cancer-predisposing syndromeUncertain significance
(Feb 20, 2018)
criteria provided, single submitterVCV000819117
78.
GRCh37:
Chr11:67254521
GRCh38:
Chr11:67487050
AIPHereditary cancer-predisposing syndrome, not provided, Somatotroph adenoma
Benign/Likely benign
(Oct 25, 2020)
criteria provided, multiple submitters, no conflictsVCV000819248
79.
GRCh37:
Chr11:67254522
GRCh38:
Chr11:67487051
AIPV49MHereditary cancer-predisposing syndrome, not provided, Somatotroph adenoma
Conflicting interpretations of pathogenicity
(Dec 4, 2020)
criteria provided, conflicting interpretationsVCV000041164
80.
GRCh37:
Chr11:67254528
GRCh38:
Chr11:67487057
AIPD51NHereditary cancer-predisposing syndrome, not providedUncertain significance
(May 25, 2020)
criteria provided, multiple submitters, no conflictsVCV000819423
81.
GRCh37:
Chr11:67254530
GRCh38:
Chr11:67487059
AIPHereditary cancer-predisposing syndromeLikely benign
(Mar 20, 2018)
criteria provided, single submitterVCV000819440
82.
GRCh37:
Chr11:67254536
GRCh38:
Chr11:67487065
AIPHereditary cancer-predisposing syndrome, not providedLikely benign
(Nov 12, 2020)
criteria provided, multiple submitters, no conflictsVCV000819642
83.
GRCh37:
Chr11:67254537
GRCh38:
Chr11:67487066
AIPR54WHereditary cancer-predisposing syndrome, not providedUncertain significance
(Apr 8, 2020)
criteria provided, multiple submitters, no conflictsVCV000819659
84.
GRCh37:
Chr11:67254538
GRCh38:
Chr11:67487067
AIPR54QHereditary cancer-predisposing syndrome, not providedUncertain significance
(Oct 20, 2020)
criteria provided, multiple submitters, no conflictsVCV000819687
85.
GRCh37:
Chr11:67254540
GRCh38:
Chr11:67487069
AIPA55Tnot providedUncertain significance
(Jan 16, 2020)
criteria provided, single submitterVCV001023228
86.
GRCh37:
Chr11:67254541
GRCh38:
Chr11:67487070
AIPA55Vnot providedUncertain significance
(May 12, 2020)
criteria provided, single submitterVCV001022659
87.
GRCh37:
Chr11:67254543
GRCh38:
Chr11:67487072
AIPR56CSomatotroph adenoma, not providedUncertain significance
(May 12, 2020)
criteria provided, multiple submitters, no conflictsVCV000877266
88.
GRCh37:
Chr11:67254543
GRCh38:
Chr11:67487072
AIPR56SSomatotroph adenomaLikely pathogenic
(Jun 21, 2012)
no assertion criteria providedVCV000041165
89.
GRCh37:
Chr11:67254544
GRCh38:
Chr11:67487073
AIPR56Hnot providedUncertain significance
(Oct 28, 2019)
criteria provided, single submitterVCV000964401
90.
GRCh37:
Chr11:67254546
GRCh38:
Chr11:67487075
AIPG57Snot providedUncertain significance
(May 12, 2020)
criteria provided, single submitterVCV001035289
91.
GRCh37:
Chr11:67254551
GRCh38:
Chr11:67487080
AIPnot providedLikely benign
(Dec 13, 2019)
criteria provided, single submitterVCV001078767
92.
GRCh37:
Chr11:67254551
GRCh38:
Chr11:67487080
AIPK58NHereditary cancer-predisposing syndrome, not provided, Somatotroph adenoma
Uncertain significance
(Jan 14, 2020)
criteria provided, multiple submitters, no conflictsVCV000041166
93.
GRCh37:
Chr11:67254552
GRCh38:
Chr11:67487081
AIPP59Snot providedUncertain significance
(Aug 24, 2020)
criteria provided, single submitterVCV000859123
94.
GRCh37:
Chr11:67254559
GRCh38:
Chr11:67487088
AIPE2G, E61Gnot providedUncertain significance
(Sep 23, 2020)
criteria provided, single submitterVCV001005479
95.
GRCh37:
Chr11:67254560
GRCh38:
Chr11:67487089
AIPnot providedLikely benign
(Sep 28, 2019)
criteria provided, single submitterVCV001135824
96.
GRCh37:
Chr11:67254565
GRCh38:
Chr11:67487094
AIPI4N, I63Nnot providedUncertain significance
(Jul 21, 2020)
criteria provided, single submitterVCV001000149
97.
GRCh37:
Chr11:67254569
GRCh38:
Chr11:67487098
AIPnot providedLikely benign
(Aug 20, 2020)
criteria provided, single submitterVCV001079361
98.
GRCh37:
Chr11:67254575
GRCh38:
Chr11:67487104
AIPnot providedLikely benign
(Oct 12, 2019)
criteria provided, single submitterVCV001093540
99.
GRCh37:
Chr11:67254582
GRCh38:
Chr11:67487111
AIPK69E, K10EHereditary cancer-predisposing syndrome, not providedUncertain significance
(Aug 20, 2020)
criteria provided, multiple submitters, no conflictsVCV000820621
100.
GRCh37:
Chr11:67254595
GRCh38:
Chr11:67487124
AIPW14*, W73*Hereditary cancer-predisposing syndromePathogenic
(Sep 5, 2019)
criteria provided, single submitterVCV000820837
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