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Items: 1 to 100 of 2192

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr10:86194737-90910559
GRCh38:
Chr10:84434981-89150802
See casesPathogenic
(Aug 12, 2011)
criteria provided, single submitterVCV000059703
2.
GRCh37:
Chr10:88514773-89725239
GRCh38:
Chr10:86755016-87965482
Generalized juvenile polyposis/juvenile polyposis coliPathogenic
(Mar 6, 2019)
criteria provided, single submitterVCV000661198
3.
GRCh37:
Chr10:88598623-89725239
GRCh38:
Chr10:86838866-87965482
Generalized juvenile polyposis/juvenile polyposis coliPathogenic
(Nov 1, 2018)
criteria provided, single submitterVCV000646972
4.
GRCh37:
Chr10:88635625-89653886
GRCh38:
Chr10:86875868-87894129
PTEN hamartoma tumor syndromePathogenic
(Sep 17, 2018)
criteria provided, single submitterVCV000660158
5.
GRCh37:
Chr10:89590587-90376982
GRCh38:
Chr10:87830830-88617225
PTEN, RNLS, ATAD1, LIPJ, KLLNPoly (ADP-Ribose) polymerase inhibitor responsedrug response
(Nov 27, 2017)
no assertion criteria providedVCV000523155
6.
GRCh37:
Chr10:89622885
GRCh38:
Chr10:87863128
PTEN, KLLNnot providedUncertain significance
(Jul 9, 2014)
criteria provided, single submitterVCV000189461
7.
GRCh37:
Chr10:89622888
GRCh38:
Chr10:87863131
PTEN, KLLNnot providedUncertain significance
(Aug 30, 2019)
criteria provided, multiple submitters, no conflictsVCV000488770
8.
GRCh37:
Chr10:89622891
GRCh38:
Chr10:87863134
PTEN, KLLNnot providedUncertain significance
(Dec 1, 2015)
criteria provided, single submitterVCV000488849
9.
GRCh37:
Chr10:89622896
GRCh38:
Chr10:87863139
PTEN, KLLNnot specifiedUncertain significance
(Mar 30, 2015)
criteria provided, single submitterVCV000503507
10.
GRCh37:
Chr10:89622902
GRCh38:
Chr10:87863145
PTEN, KLLNnot providedUncertain significance
(Dec 31, 2014)
criteria provided, single submitterVCV000503638
11.
GRCh37:
Chr10:89622905
GRCh38:
Chr10:87863148
PTEN, KLLNnot providedUncertain significance
(Jun 21, 2017)
criteria provided, single submitterVCV000488905
12.
GRCh37:
Chr10:89622915
GRCh38:
Chr10:87863158
PTEN, KLLNnot specified, not provided, PTEN hamartoma tumor syndrome
Benign
(Jun 2, 2017)
reviewed by expert panel
FDA Recognized Database
VCV000127667
13.
GRCh37:
Chr10:89622916
GRCh38:
Chr10:87863159
PTEN, KLLNnot providedUncertain significance
(May 12, 2015)
criteria provided, single submitterVCV000488761
14.
GRCh37:
Chr10:89622918-89624325
GRCh38:
Chr10:87863161-87864568
PTEN, KLLNPTEN hamartoma tumor syndromeUncertain significance
(Feb 27, 2018)
criteria provided, single submitterVCV000583889
15.
GRCh37:
Chr10:89622919
GRCh38:
Chr10:87863162
KLLN, PTENnot providedUncertain significance
(Aug 16, 2016)
criteria provided, single submitterVCV000488860
16.
GRCh37:
Chr10:89622921
GRCh38:
Chr10:87863164
PTEN, KLLNnot specifiedUncertain significance
(Apr 28, 2017)
criteria provided, single submitterVCV000439287
17.
GRCh37:
Chr10:89622925
GRCh38:
Chr10:87863168
PTEN, KLLNnot providedUncertain significance
(Mar 26, 2016)
criteria provided, single submitterVCV000488886
18.
GRCh37:
Chr10:89622928-89624315
GRCh38:
Chr10:87863171-87864558
PTEN, KLLNPTEN hamartoma tumor syndromePathogenic
(Jan 28, 2019)
criteria provided, single submitterVCV000584299
19.
GRCh37:
Chr10:89622928
GRCh38:
Chr10:87863171
PTEN, KLLNnot providedUncertain significance
(Oct 11, 2017)
criteria provided, single submitterVCV000488783
20.
GRCh37:
Chr10:89622931
GRCh38:
Chr10:87863174
PTEN, KLLNnot providedUncertain significance
(Oct 9, 2017)
criteria provided, single submitterVCV000488754
21.
GRCh37:
Chr10:89622933
GRCh38:
Chr10:87863176
PTEN, KLLNnot providedUncertain significance
(Sep 26, 2016)
criteria provided, single submitterVCV000488713
22.
GRCh37:
Chr10:89622936
GRCh38:
Chr10:87863179
PTEN, KLLNnot specifiedUncertain significance
(Oct 13, 2016)
criteria provided, single submitterVCV000234639
23.
GRCh37:
Chr10:89622938-89622939
GRCh38:
Chr10:87863181-87863182
PTEN, KLLNnot providedUncertain significance
(Feb 22, 2019)
criteria provided, single submitterVCV000801274
24.
GRCh37:
Chr10:89622939
GRCh38:
Chr10:87863182
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Mar 17, 2018)
criteria provided, multiple submitters, no conflictsVCV000488910
25.
GRCh37:
Chr10:89622939
GRCh38:
Chr10:87863182
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Sep 7, 2017)
criteria provided, single submitterVCV000141821
26.
GRCh37:
Chr10:89622941
GRCh38:
Chr10:87863184
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(May 9, 2018)
criteria provided, single submitterVCV000818802
27.
GRCh37:
Chr10:89622942
GRCh38:
Chr10:87863185
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jun 7, 2018)
criteria provided, single submitterVCV000818794
28.
GRCh37:
Chr10:89622945
GRCh38:
Chr10:87863188
PTEN, KLLNnot providedUncertain significance
(May 2, 2016)
criteria provided, single submitterVCV000488901
29.
GRCh37:
Chr10:89622951
GRCh38:
Chr10:87863194
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(May 2, 2018)
criteria provided, multiple submitters, no conflictsVCV000488934
30.
GRCh37:
Chr10:89622960
GRCh38:
Chr10:87863203
PTEN, KLLNnot providedUncertain significance
(Jan 26, 2015)
criteria provided, single submitterVCV000503639
31.
GRCh37:
Chr10:89622964
GRCh38:
Chr10:87863207
PTEN, KLLNnot specifiedUncertain significanceno assertion criteria providedVCV000492717
32.
GRCh37:
Chr10:89622965
GRCh38:
Chr10:87863208
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Oct 16, 2019)
criteria provided, single submitterVCV000818721
33.
GRCh37:
Chr10:89622970
GRCh38:
Chr10:87863213
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Oct 24, 2019)
criteria provided, single submitterVCV000141062
34.
GRCh37:
Chr10:89622976-89622977
GRCh38:
Chr10:87863219-87863220
PTEN, KLLNHereditary cancer-predisposing syndrome, not specifiedUncertain significance
(Sep 27, 2018)
criteria provided, multiple submitters, no conflictsVCV000189445
35.
GRCh37:
Chr10:89622980
GRCh38:
Chr10:87863223
PTEN, KLLNCowden syndrome 1, Macrocephaly/autism syndrome, Malignant tumor of prostate,
Glioma susceptibility 2, VACTERL association with hydrocephalus, PTEN hamartoma tumor syndrome,
Meningioma, familial, not provided
Uncertain significance
(Oct 31, 2018)
criteria provided, multiple submitters, no conflictsVCV000488964
36.
GRCh37:
Chr10:89622982
GRCh38:
Chr10:87863225
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Feb 23, 2018)
criteria provided, single submitterVCV000818681
37.
GRCh37:
Chr10:89622983
GRCh38:
Chr10:87863226
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jul 5, 2018)
criteria provided, single submitterVCV000127666
38.
GRCh37:
Chr10:89622984
GRCh38:
Chr10:87863227
KLLN, PTENPTEN hamartoma tumor syndrome, not providedUncertain significance
(May 28, 2019)
criteria provided, multiple submitters, no conflictsVCV000189522
39.
GRCh37:
Chr10:89622986
GRCh38:
Chr10:87863229
PTEN, KLLNnot providedUncertain significance
(Jul 28, 2015)
criteria provided, single submitterVCV000488776
40.
GRCh37:
Chr10:89622989
GRCh38:
Chr10:87863232
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jan 25, 2019)
criteria provided, single submitterVCV000818672
41.
GRCh37:
Chr10:89622989
GRCh38:
Chr10:87863232
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Dec 26, 2017)
criteria provided, single submitterVCV000818671
42.
GRCh37:
Chr10:89622991
GRCh38:
Chr10:87863234
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Apr 23, 2018)
criteria provided, single submitterVCV000186644
43.
GRCh37:
Chr10:89622991
GRCh38:
Chr10:87863234
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Feb 25, 2019)
criteria provided, multiple submitters, no conflictsVCV000127665
44.
GRCh37:
Chr10:89622992
GRCh38:
Chr10:87863235
PTEN, KLLNnot specifiedUncertain significance
(Mar 10, 2016)
criteria provided, single submitterVCV000234894
45.
GRCh37:
Chr10:89622992
GRCh38:
Chr10:87863235
PTEN, KLLNnot providedUncertain significance
(Jan 3, 2014)
criteria provided, single submitterVCV000189526
46.
GRCh37:
Chr10:89623000
GRCh38:
Chr10:87863243
PTEN, KLLNnot providedUncertain significance
(Sep 29, 2016)
criteria provided, single submitterVCV000488867
47.
GRCh37:
Chr10:89623002
GRCh38:
Chr10:87863245
PTEN, KLLNnot providedUncertain significance
(Oct 17, 2017)
criteria provided, single submitterVCV000488868
48.
GRCh37:
Chr10:89623004
GRCh38:
Chr10:87863247
PTEN, KLLNnot providedUncertain significance
(Apr 4, 2018)
criteria provided, single submitterVCV000488935
49.
GRCh37:
Chr10:89623005
GRCh38:
Chr10:87863248
PTEN, KLLNnot providedUncertain significance
(Nov 9, 2016)
criteria provided, single submitterVCV000488954
50.
GRCh37:
Chr10:89623005
GRCh38:
Chr10:87863248
KLLN, PTENnot providedUncertain significance
(May 25, 2020)
criteria provided, multiple submitters, no conflictsVCV000488773
51.
GRCh37:
Chr10:89623010
GRCh38:
Chr10:87863253
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Oct 30, 2014)
criteria provided, single submitterVCV000186991
52.
GRCh37:
Chr10:89623012
GRCh38:
Chr10:87863255
KLLN, PTENHereditary cancer-predisposing syndromeUncertain significance
(Apr 2, 2014)
criteria provided, single submitterVCV000142999
53.
GRCh37:
Chr10:89623014
GRCh38:
Chr10:87863257
PTEN, KLLNnot providedUncertain significance
(Oct 27, 2017)
criteria provided, multiple submitters, no conflictsVCV000488850
54.
GRCh37:
Chr10:89623016
GRCh38:
Chr10:87863259
KLLN, PTENnot providedUncertain significance
(Aug 11, 2017)
criteria provided, single submitterVCV000189521
55.
GRCh37:
Chr10:89623018
GRCh38:
Chr10:87863261
PTEN, KLLNnot providedUncertain significance
(Apr 21, 2014)
criteria provided, single submitterVCV000189469
56.
GRCh37:
Chr10:89623019
GRCh38:
Chr10:87863262
KLLN, PTENnot providedUncertain significance
(Apr 8, 2020)
criteria provided, multiple submitters, no conflictsVCV000234396
57.
GRCh37:
Chr10:89623020
GRCh38:
Chr10:87863263
PTEN, KLLNnot providedUncertain significance
(May 11, 2015)
criteria provided, single submitterVCV000488714
58.
GRCh37:
Chr10:89623021
GRCh38:
Chr10:87863264
PTEN, KLLNnot providedUncertain significance
(Jul 10, 2017)
criteria provided, single submitterVCV000488715
59.
GRCh37:
Chr10:89623024
GRCh38:
Chr10:87863267
PTEN, KLLNnot providedUncertain significance
(Nov 29, 2017)
criteria provided, single submitterVCV000234473
60.
GRCh37:
Chr10:89623027-89623038
GRCh38:
Chr10:87863270-87863281
PTEN, KLLNHereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, not provided
Likely benign
(Mar 5, 2019)
reviewed by expert panel
FDA Recognized Database
VCV000189433
61.
GRCh37:
Chr10:89623034
GRCh38:
Chr10:87863277
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Nov 30, 2019)
criteria provided, multiple submitters, no conflictsVCV000488900
62.
GRCh37:
Chr10:89623036-89623038
GRCh38:
Chr10:87863279-87863281
KLLN, PTENHereditary cancer-predisposing syndromeUncertain significance
(Apr 26, 2014)
criteria provided, single submitterVCV000142982
63.
GRCh37:
Chr10:89623036
GRCh38:
Chr10:87863279
PTEN, KLLNMacrocephaly/autism syndrome, Meningioma, familial, Glioma susceptibility 2,
Cowden syndrome 1, Malignant tumor of prostate, VACTERL association with hydrocephalus,
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, not provided,
PTEN hamartoma tumor syndrome
Uncertain significance
(Mar 23, 2020)
reviewed by expert panel
FDA Recognized Database
VCV000127663
64.
GRCh37:
Chr10:89623045-89623061
GRCh38:
Chr10:87863288-87863304
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Apr 8, 2019)
criteria provided, single submitterVCV000818504
65.
GRCh37:
Chr10:89623045
GRCh38:
Chr10:87863288
PTEN, KLLNnot providedUncertain significance
(Dec 23, 2017)
criteria provided, multiple submitters, no conflictsVCV000488716
66.
GRCh37:
Chr10:89623047-89623048
GRCh38:
Chr10:87863290-87863291
PTEN, KLLNnot providedUncertain significance
(Aug 29, 2016)
criteria provided, single submitterVCV000503748
67.
GRCh37:
Chr10:89623047
GRCh38:
Chr10:87863290
PTEN, KLLNHereditary cancer-predisposing syndrome, not providedUncertain significance
(May 7, 2018)
criteria provided, multiple submitters, no conflictsVCV000142652
68.
GRCh37:
Chr10:89623050
GRCh38:
Chr10:87863293
PTEN, KLLNHereditary cancer-predisposing syndrome, not provided, Cowden syndrome 1
Uncertain significance
(Feb 13, 2018)
criteria provided, multiple submitters, no conflictsVCV000142844
69.
GRCh37:
Chr10:89623052
GRCh38:
Chr10:87863295
PTEN, KLLNnot providedUncertain significance
(Sep 19, 2016)
criteria provided, single submitterVCV000488939
70.
GRCh37:
Chr10:89623053
GRCh38:
Chr10:87863296
PTEN, KLLNnot providedUncertain significance
(Mar 7, 2016)
criteria provided, single submitterVCV000488866
71.
GRCh37:
Chr10:89623054
GRCh38:
Chr10:87863297
PTEN, KLLNnot providedUncertain significance
(Jan 3, 2017)
criteria provided, single submitterVCV000488786
72.
GRCh37:
Chr10:89623054
GRCh38:
Chr10:87863297
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(May 17, 2018)
criteria provided, single submitterVCV000141170
73.
GRCh37:
Chr10:89623056
GRCh38:
Chr10:87863299
PTEN, KLLNHereditary cancer-predisposing syndrome, not provided, Cowden syndrome 1
Uncertain significance
(Jul 5, 2018)
criteria provided, multiple submitters, no conflictsVCV000140783
74.
GRCh37:
Chr10:89623056
GRCh38:
Chr10:87863299
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome,
Cowden syndrome 1
Likely benign
(Mar 23, 2020)
reviewed by expert panel
FDA Recognized Database
VCV000127662
75.
GRCh37:
Chr10:89623058
GRCh38:
Chr10:87863301
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Aug 14, 2018)
criteria provided, single submitterVCV000818474
76.
GRCh37:
Chr10:89623061
GRCh38:
Chr10:87863304
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Dec 6, 2018)
criteria provided, single submitterVCV000822264
77.
GRCh37:
Chr10:89623065-89623066
GRCh38:
Chr10:87863308-87863309
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jan 2, 2019)
criteria provided, single submitterVCV000818444
78.
GRCh37:
Chr10:89623072
GRCh38:
Chr10:87863315
PTEN, KLLNnot provided, Meningioma, familial, Cowden syndrome 1,
PTEN hamartoma tumor syndrome, Malignant tumor of prostate, Macrocephaly/autism syndrome,
Glioma susceptibility 2, VACTERL association with hydrocephalus, Hereditary cancer-predisposing syndrome
Uncertain significance
(Aug 12, 2019)
criteria provided, multiple submitters, no conflictsVCV000187362
79.
GRCh37:
Chr10:89623073
GRCh38:
Chr10:87863316
PTEN, KLLNnot providedUncertain significance
(Feb 17, 2017)
criteria provided, single submitterVCV000488717
80.
GRCh37:
Chr10:89623074
GRCh38:
Chr10:87863317
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jun 10, 2019)
criteria provided, single submitterVCV000818430
81.
GRCh37:
Chr10:89623075
GRCh38:
Chr10:87863318
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jul 18, 2018)
criteria provided, single submitterVCV000818427
82.
GRCh37:
Chr10:89623075
GRCh38:
Chr10:87863318
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jul 30, 2019)
criteria provided, single submitterVCV000818426
83.
GRCh37:
Chr10:89623081
GRCh38:
Chr10:87863324
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Feb 20, 2019)
criteria provided, single submitterVCV000822248
84.
GRCh37:
Chr10:89623081
GRCh38:
Chr10:87863324
KLLN, PTENHereditary cancer-predisposing syndromeUncertain significance
(Feb 14, 2019)
criteria provided, single submitterVCV000187000
85.
GRCh37:
Chr10:89623082
GRCh38:
Chr10:87863325
KLLN, PTENnot providedUncertain significance
(Nov 11, 2016)
criteria provided, single submitterVCV000234900
86.
GRCh37:
Chr10:89623083
GRCh38:
Chr10:87863326
PTEN, KLLNnot providedUncertain significance
(Mar 10, 2016)
criteria provided, single submitterVCV000488748
87.
GRCh37:
Chr10:89623084
GRCh38:
Chr10:87863327
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Dec 20, 2018)
criteria provided, multiple submitters, no conflictsVCV000234867
88.
GRCh37:
Chr10:89623084-89623085
GRCh38:
Chr10:87863327-87863328
KLLN, PTENnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Nov 20, 2015)
criteria provided, multiple submitters, no conflictsVCV000234632
89.
GRCh37:
Chr10:89623084
GRCh38:
Chr10:87863327
PTEN, KLLNHereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, not provided,
not specified
Likely benign
(Apr 6, 2018)
reviewed by expert panel
FDA Recognized Database
VCV000127661
90.
GRCh37:
Chr10:89623085
GRCh38:
Chr10:87863328
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Jul 2, 2018)
criteria provided, single submitterVCV000822240
91.
GRCh37:
Chr10:89623088
GRCh38:
Chr10:87863331
KLLN, PTENnot providedUncertain significance
(Apr 10, 2015)
criteria provided, single submitterVCV000488755
92.
GRCh37:
Chr10:89623089
GRCh38:
Chr10:87863332
PTEN, KLLNnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Apr 5, 2019)
criteria provided, multiple submitters, no conflictsVCV000141864
93.
GRCh37:
Chr10:89623090
GRCh38:
Chr10:87863333
PTEN, KLLNnot providedUncertain significance
(Dec 2, 2019)
criteria provided, multiple submitters, no conflictsVCV000488938
94.
GRCh37:
Chr10:89623091-89623092
GRCh38:
Chr10:87863334-87863335
PTEN, KLLNHereditary cancer-predisposing syndromeUncertain significance
(Aug 6, 2014)
criteria provided, single submitterVCV000189434
95.
GRCh37:
Chr10:89623093
GRCh38:
Chr10:87863336
KLLN, PTENHereditary cancer-predisposing syndromeUncertain significance
(Mar 26, 2014)
criteria provided, single submitterVCV000142892
96.
GRCh37:
Chr10:89623096
GRCh38:
Chr10:87863339
PTEN, KLLNnot providedUncertain significance
(Jun 10, 2015)
criteria provided, single submitterVCV000503509
97.
GRCh37:
Chr10:89623104
GRCh38:
Chr10:87863347
PTEN, KLLNnot providedUncertain significance
(Jun 30, 2016)
criteria provided, single submitterVCV000488922
98.
GRCh37:
Chr10:89623105
GRCh38:
Chr10:87863348
PTEN, KLLNnot providedUncertain significance
(Dec 11, 2015)
criteria provided, single submitterVCV000234686
99.
GRCh37:
Chr10:89623106
GRCh38:
Chr10:87863349
PTEN, KLLNnot provided, not specifiedUncertain significance
(Dec 11, 2017)
criteria provided, multiple submitters, no conflictsVCV000503505
100.
GRCh37:
Chr10:89623114
GRCh38:
Chr10:87863357
PTEN, KLLNnot providedUncertain significance
(Jul 30, 2018)
criteria provided, multiple submitters, no conflictsVCV000503511
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