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Items: 1 to 100 of 1954

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr10:89623292
GRCh38:
Chr10:87863535
PTENHereditary cancer-predisposing syndromeUncertain significance
(Apr 30, 2019)
criteria provided, single submitterVCV000187183
2.
GRCh37:
Chr10:89623293
GRCh38:
Chr10:87863536
PTENnot providedUncertain significance
(Jan 20, 2015)
criteria provided, single submitterVCV000503643
3.
GRCh37:
Chr10:89623293
GRCh38:
Chr10:87863536
PTENHereditary cancer-predisposing syndromeUncertain significance
(Nov 14, 2018)
criteria provided, single submitterVCV000187033
4.
GRCh37:
Chr10:89623294
GRCh38:
Chr10:87863537
PTENnot providedUncertain significance
(Sep 14, 2018)
criteria provided, single submitterVCV000488718
5.
GRCh37:
Chr10:89623296
GRCh38:
Chr10:87863539
PTENHereditary cancer-predisposing syndrome, not providedUncertain significance
(Apr 12, 2020)
criteria provided, multiple submitters, no conflictsVCV000141717
6.
GRCh37:
Chr10:89623297
GRCh38:
Chr10:87863540
PTENnot specified, not providedUncertain significance
(Oct 24, 2019)
criteria provided, multiple submitters, no conflictsVCV000488719
7.
GRCh37:
Chr10:89623299
GRCh38:
Chr10:87863542
PTENnot specifiedUncertain significance
(Jan 18, 2019)
criteria provided, single submitterVCV000928905
8.
GRCh37:
Chr10:89623299
GRCh38:
Chr10:87863542
PTENnot providedUncertain significance
(Jul 2, 2018)
criteria provided, single submitterVCV000488759
9.
GRCh37:
Chr10:89623301
GRCh38:
Chr10:87863544
PTENHereditary cancer-predisposing syndromeUncertain significance
(Sep 23, 2019)
criteria provided, single submitterVCV000823136
10.
GRCh37:
Chr10:89623301
GRCh38:
Chr10:87863544
PTENnot providedUncertain significance
(Feb 8, 2017)
criteria provided, single submitterVCV000488765
11.
GRCh37:
Chr10:89623303
GRCh38:
Chr10:87863546
PTENnot providedUncertain significance
(May 22, 2015)
criteria provided, single submitterVCV000189491
12.
GRCh37:
Chr10:89623305
GRCh38:
Chr10:87863548
PTENnot providedUncertain significance
(Dec 26, 2019)
criteria provided, single submitterVCV000993122
13.
GRCh37:
Chr10:89623305
GRCh38:
Chr10:87863548
PTENnot specified, Hereditary cancer-predisposing syndromeUncertain significance
(Oct 18, 2019)
criteria provided, multiple submitters, no conflictsVCV000449087
14.
GRCh37:
Chr10:89623305
GRCh38:
Chr10:87863548
PTENHereditary cancer-predisposing syndrome, not specifiedUncertain significance
(Jun 21, 2018)
criteria provided, single submitterVCV000187364
15.
GRCh37:
Chr10:89623306
GRCh38:
Chr10:87863549
PTENnot provided, not specified, PTEN hamartoma tumor syndrome
Uncertain significance
(May 24, 2021)
criteria provided, multiple submitters, no conflictsVCV000189492
16.
GRCh37:
Chr10:89623308
GRCh38:
Chr10:87863551
PTENnot specified, Hereditary cancer-predisposing syndromeUncertain significance
(Jul 16, 2020)
criteria provided, multiple submitters, no conflictsVCV000419934
17.
GRCh37:
Chr10:89623309
GRCh38:
Chr10:87863552
PTENHereditary cancer-predisposing syndrome, not providedUncertain significance
(Dec 19, 2018)
criteria provided, multiple submitters, no conflictsVCV000495812
18.
GRCh37:
Chr10:89623311
GRCh38:
Chr10:87863554
PTENnot providedUncertain significance
(Jan 16, 2020)
criteria provided, single submitterVCV000488750
19.
GRCh37:
Chr10:89623312
GRCh38:
Chr10:87863555
PTENnot providedUncertain significance
(Sep 26, 2016)
criteria provided, single submitterVCV000488943
20.
GRCh37:
Chr10:89623314
GRCh38:
Chr10:87863557
PTENnot specified, not providedUncertain significance
(Feb 14, 2019)
criteria provided, multiple submitters, no conflictsVCV000488720
21.
GRCh37:
Chr10:89623317
GRCh38:
Chr10:87863560
PTENnot specified, not providedUncertain significance
(Jan 14, 2020)
criteria provided, multiple submitters, no conflictsVCV000488768
22.
GRCh37:
Chr10:89623317
GRCh38:
Chr10:87863560
PTENnot provided, Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome,
not specified
Likely benign
(Jul 25, 2018)
reviewed by expert panel
FDA Recognized Database
VCV000127681
23.
GRCh37:
Chr10:89623319-89623320
GRCh38:
Chr10:87863562-87863563
PTENHereditary cancer-predisposing syndromeUncertain significance
(Oct 29, 2019)
criteria provided, single submitterVCV000822971
24.
GRCh37:
Chr10:89623319-89623320
GRCh38:
Chr10:87863562-87863563
PTENnot providedUncertain significance
(Jan 10, 2019)
criteria provided, single submitterVCV000189436
25.
GRCh37:
Chr10:89623319
GRCh38:
Chr10:87863562
PTENnot providedUncertain significance
(Feb 25, 2014)
criteria provided, single submitterVCV000127680
26.
GRCh37:
Chr10:89623320
GRCh38:
Chr10:87863563
PTENHereditary cancer-predisposing syndromeUncertain significance
(Oct 18, 2019)
criteria provided, single submitterVCV000822982
27.
GRCh37:
Chr10:89623320-89623341
GRCh38:
Chr10:87863563-87863584
PTENHereditary cancer-predisposing syndromeUncertain significance
(Nov 23, 2018)
criteria provided, single submitterVCV000822925
28.
GRCh37:
Chr10:89623320-89623321
GRCh38:
Chr10:87863563-87863564
PTENnot providedUncertain significance
(Feb 4, 2016)
criteria provided, single submitterVCV000503732
29.
GRCh37:
Chr10:89623320
GRCh38:
Chr10:87863563
PTENHereditary cancer-predisposing syndrome, not specifiedUncertain significance
(Dec 17, 2019)
criteria provided, multiple submitters, no conflictsVCV000422946
30.
GRCh37:
Chr10:89623322-89623323
GRCh38:
Chr10:87863565-87863566
PTENHereditary cancer-predisposing syndromeUncertain significance
(May 24, 2018)
criteria provided, single submitterVCV000822917
31.
GRCh37:
Chr10:89623322-89623323
GRCh38:
Chr10:87863565-87863566
PTENnot providedUncertain significance
(Feb 19, 2016)
criteria provided, single submitterVCV000503734
32.
GRCh37:
Chr10:89623322
GRCh38:
Chr10:87863565
PTENnot providedUncertain significance
(Jan 3, 2018)
criteria provided, multiple submitters, no conflictsVCV000127679
33.
GRCh37:
Chr10:89623323
GRCh38:
Chr10:87863566
PTENHereditary cancer-predisposing syndromeUncertain significance
(Jul 24, 2018)
criteria provided, single submitterVCV000822924
34.
GRCh37:
Chr10:89623323
GRCh38:
Chr10:87863566
PTENHereditary cancer-predisposing syndromeUncertain significance
(Oct 18, 2019)
criteria provided, single submitterVCV000822915
35.
GRCh37:
Chr10:89623323-89623324
GRCh38:
Chr10:87863566-87863567
PTENnot providedUncertain significance
(May 8, 2020)
criteria provided, single submitterVCV000619909
36.
GRCh37:
Chr10:89623323
GRCh38:
Chr10:87863566
PTENnot specified, not providedUncertain significance
(Dec 2, 2019)
criteria provided, multiple submitters, no conflictsVCV000421785
37.
GRCh37:
Chr10:89623323
GRCh38:
Chr10:87863566
PTENnot specified, not provided, PTEN hamartoma tumor syndrome,
none provided
Benign
(Sep 14, 2016)
reviewed by expert panel
FDA Recognized Database
VCV000138837
38.
GRCh37:
Chr10:89623324
GRCh38:
Chr10:87863567
PTENHereditary cancer-predisposing syndromeUncertain significance
(Mar 29, 2019)
criteria provided, single submitterVCV000822916
39.
GRCh37:
Chr10:89623325
GRCh38:
Chr10:87863568
PTENnot providedUncertain significance
(Jun 2, 2016)
criteria provided, single submitterVCV000495811
40.
GRCh37:
Chr10:89623329
GRCh38:
Chr10:87863572
PTENnot providedUncertain significance
(May 20, 2020)
criteria provided, single submitterVCV001047923
41.
GRCh37:
Chr10:89623329
GRCh38:
Chr10:87863572
PTENnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Oct 13, 2015)
criteria provided, multiple submitters, no conflictsVCV000141748
42.
GRCh37:
Chr10:89623330-89623331
GRCh38:
Chr10:87863573-87863574
PTENHereditary cancer-predisposing syndromeUncertain significance
(Jul 5, 2019)
criteria provided, single submitterVCV000822846
43.
GRCh37:
Chr10:89623334
GRCh38:
Chr10:87863577
PTENnot providedUncertain significance
(Aug 15, 2016)
criteria provided, single submitterVCV000503747
44.
GRCh37:
Chr10:89623334
GRCh38:
Chr10:87863577
PTENnot providedUncertain significance
(Nov 9, 2015)
criteria provided, single submitterVCV000189493
45.
GRCh37:
Chr10:89623336
GRCh38:
Chr10:87863579
PTENnot providedUncertain significance
(Mar 30, 2018)
criteria provided, single submitterVCV000488721
46.
GRCh37:
Chr10:89623339
GRCh38:
Chr10:87863582
PTENHereditary cancer-predisposing syndromeUncertain significance
(Apr 22, 2014)
criteria provided, single submitterVCV000142883
47.
GRCh37:
Chr10:89623351-89623352
GRCh38:
Chr10:87863594-87863595
PTENHereditary cancer-predisposing syndromeUncertain significance
(Aug 27, 2014)
criteria provided, single submitterVCV000189437
48.
GRCh37:
Chr10:89623352-89623358
GRCh38:
Chr10:87863595-87863601
PTENnot providedUncertain significance
(Apr 11, 2016)
criteria provided, single submitterVCV000503739
49.
GRCh37:
Chr10:89623354
GRCh38:
Chr10:87863597
PTENnot providedUncertain significance
(Nov 24, 2018)
criteria provided, single submitterVCV000488914
50.
GRCh37:
Chr10:89623355
GRCh38:
Chr10:87863598
PTENnot providedUncertain significance
(Dec 9, 2019)
criteria provided, single submitterVCV001048098
51.
GRCh37:
Chr10:89623357
GRCh38:
Chr10:87863600
PTENnot providedUncertain significance
(May 19, 2014)
criteria provided, single submitterVCV000189494
52.
GRCh37:
Chr10:89623358
GRCh38:
Chr10:87863601
PTENnot providedUncertain significance
(Jul 20, 2018)
criteria provided, single submitterVCV000189495
53.
GRCh37:
Chr10:89623358
GRCh38:
Chr10:87863601
PTENVACTERL association with hydrocephalus, Glioma susceptibility 2, Cowden syndrome 1,
Malignant tumor of prostate, Meningioma, familial, PTEN hamartoma tumor syndrome,
Macrocephaly/autism syndrome, not provided, PTEN hamartoma tumor syndrome,
Hereditary cancer-predisposing syndrome, not specified ...see more
Uncertain significance
(May 19, 2021)
criteria provided, multiple submitters, no conflictsVCV000141949
54.
GRCh37:
Chr10:89623360
GRCh38:
Chr10:87863603
PTENnot specifiedUncertain significance
(Apr 15, 2016)
criteria provided, single submitterVCV000488892
55.
GRCh37:
Chr10:89623362
GRCh38:
Chr10:87863605
PTENnot providedUncertain significance
(Sep 12, 2018)
criteria provided, single submitterVCV000488857
56.
GRCh37:
Chr10:89623363
GRCh38:
Chr10:87863606
PTENnot providedUncertain significance
(Nov 10, 2017)
criteria provided, single submitterVCV000488736
57.
GRCh37:
Chr10:89623364
GRCh38:
Chr10:87863607
PTENHereditary cancer-predisposing syndromeUncertain significance
(Jul 10, 2019)
criteria provided, single submitterVCV000822613
58.
GRCh37:
Chr10:89623364
GRCh38:
Chr10:87863607
PTENnot providedUncertain significance
(Feb 5, 2016)
criteria provided, single submitterVCV000234823
59.
GRCh37:
Chr10:89623364
GRCh38:
Chr10:87863607
PTENHereditary cancer-predisposing syndromeUncertain significance
(Mar 5, 2014)
criteria provided, single submitterVCV000141383
60.
GRCh37:
Chr10:89623365
GRCh38:
Chr10:87863608
PTENHereditary cancer-predisposing syndromeUncertain significance
(Nov 25, 2019)
criteria provided, single submitterVCV000822606
61.
GRCh37:
Chr10:89623365
GRCh38:
Chr10:87863608
PTENnot providedUncertain significance
(Jan 31, 2017)
criteria provided, single submitterVCV000189496
62.
GRCh37:
Chr10:89623365
GRCh38:
Chr10:87863608
PTENCowden syndrome 1, PTEN hamartoma tumor syndromeUncertain significance
(Nov 28, 2018)
reviewed by expert panel
FDA Recognized Database
VCV000007845
63.
GRCh37:
Chr10:89623367
GRCh38:
Chr10:87863610
PTENnot specified, not providedUncertain significance
(Jul 10, 2020)
criteria provided, multiple submitters, no conflictsVCV000488769
64.
GRCh37:
Chr10:89623367
GRCh38:
Chr10:87863610
PTENnot providedUncertain significance
(Mar 17, 2016)
criteria provided, single submitterVCV000234457
65.
GRCh37:
Chr10:89623368
GRCh38:
Chr10:87863611
PTENnot providedUncertain significance
(Nov 10, 2017)
criteria provided, multiple submitters, no conflictsVCV000488764
66.
GRCh37:
Chr10:89623370
GRCh38:
Chr10:87863613
PTENnot providedUncertain significance
(Aug 24, 2016)
criteria provided, single submitterVCV000495810
67.
GRCh37:
Chr10:89623370
GRCh38:
Chr10:87863613
PTENnot provided, not specifiedUncertain significance
(Nov 6, 2020)
criteria provided, multiple submitters, no conflictsVCV000127678
68.
GRCh37:
Chr10:89623372
GRCh38:
Chr10:87863615
PTENnot providedUncertain significance
(Dec 5, 2016)
criteria provided, single submitterVCV000488959
69.
GRCh37:
Chr10:89623374
GRCh38:
Chr10:87863617
PTENnot providedUncertain significance
(Mar 19, 2015)
criteria provided, single submitterVCV000488747
70.
GRCh37:
Chr10:89623375
GRCh38:
Chr10:87863618
PTENnot providedUncertain significance
(Apr 6, 2018)
criteria provided, single submitterVCV000234490
71.
GRCh37:
Chr10:89623376
GRCh38:
Chr10:87863619
PTENnot providedUncertain significance
(Apr 26, 2018)
criteria provided, single submitterVCV000234486
72.
GRCh37:
Chr10:89623378
GRCh38:
Chr10:87863621
PTENnot providedUncertain significance
(Jul 13, 2016)
criteria provided, single submitterVCV000488925
73.
GRCh37:
Chr10:89623380
GRCh38:
Chr10:87863623
PTENnot providedUncertain significance
(Jun 22, 2015)
criteria provided, single submitterVCV000189407
74.
GRCh37:
Chr10:89623381
GRCh38:
Chr10:87863624
PTENnot provided, PTEN hamartoma tumor syndromeUncertain significance
(May 28, 2019)
criteria provided, multiple submitters, no conflictsVCV000189408
75.
GRCh37:
Chr10:89623383-89623385
GRCh38:
Chr10:87863626-87863628
PTENnot providedUncertain significance
(Sep 8, 2016)
criteria provided, single submitterVCV000503750
76.
GRCh37:
Chr10:89623383
GRCh38:
Chr10:87863626
PTENnot providedUncertain significance
(Mar 1, 2018)
criteria provided, single submitterVCV000127677
77.
GRCh37:
Chr10:89623387
GRCh38:
Chr10:87863630
PTENnot providedUncertain significance
(Dec 21, 2018)
criteria provided, single submitterVCV000488777
78.
GRCh37:
Chr10:89623387
GRCh38:
Chr10:87863630
PTENHereditary cancer-predisposing syndromeUncertain significance
(Feb 17, 2014)
criteria provided, single submitterVCV000141662
79.
GRCh37:
Chr10:89623389
GRCh38:
Chr10:87863632
PTENnot providedUncertain significance
(Feb 10, 2015)
criteria provided, single submitterVCV000503644
80.
GRCh37:
Chr10:89623389
GRCh38:
Chr10:87863632
PTENnot specified, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Oct 28, 2019)
criteria provided, multiple submitters, no conflictsVCV000185062
81.
GRCh37:
Chr10:89623390
GRCh38:
Chr10:87863633
PTENnot specified, not provided, PTEN hamartoma tumor syndrome
Uncertain significance
(Nov 22, 2019)
reviewed by expert panel
FDA Recognized Database
VCV000189497
82.
GRCh37:
Chr10:89623391
GRCh38:
Chr10:87863634
PTENHereditary cancer-predisposing syndromeUncertain significance
(Dec 18, 2013)
criteria provided, single submitterVCV000142124
83.
GRCh37:
Chr10:89623392
GRCh38:
Chr10:87863635
PTENCowden syndrome 1, Hereditary cancer-predisposing syndrome, Macrocephaly/autism syndrome,
PTEN hamartoma tumor syndrome, Malignant tumor of prostate, Meningioma, familial,
Glioma susceptibility 2, VACTERL association with hydrocephalus, Cowden syndrome 1,
not specified, not provided ...see more
Uncertain significance
(Mar 19, 2020)
criteria provided, multiple submitters, no conflictsVCV000127676
84.
GRCh37:
Chr10:89623394
GRCh38:
Chr10:87863637
PTENnot providedUncertain significance
(Nov 17, 2016)
criteria provided, single submitterVCV000488778
85.
GRCh37:
Chr10:89623395
GRCh38:
Chr10:87863638
PTENHereditary cancer-predisposing syndromeUncertain significance
(Mar 5, 2014)
criteria provided, single submitterVCV000141687
86.
GRCh37:
Chr10:89623399
GRCh38:
Chr10:87863642
PTENnot providedUncertain significance
(Nov 10, 2017)
criteria provided, single submitterVCV000488780
87.
GRCh37:
Chr10:89623405
GRCh38:
Chr10:87863648
PTENnot provided, VACTERL association with hydrocephalus, PTEN hamartoma tumor syndrome,
Cowden syndrome 1, Malignant tumor of prostate, Macrocephaly/autism syndrome,
Glioma susceptibility 2, Meningioma, familial
Uncertain significance
(Dec 14, 2018)
criteria provided, multiple submitters, no conflictsVCV000234510
88.
GRCh37:
Chr10:89623405
GRCh38:
Chr10:87863648
PTENnot providedUncertain significance
(Jan 27, 2014)
criteria provided, single submitterVCV000127675
89.
GRCh37:
Chr10:89623406
GRCh38:
Chr10:87863649
PTENHereditary cancer-predisposing syndromeUncertain significance
(Nov 19, 2019)
criteria provided, single submitterVCV000827511
90.
GRCh37:
Chr10:89623406
GRCh38:
Chr10:87863649
PTENHereditary cancer-predisposing syndromeUncertain significance
(Oct 23, 2019)
criteria provided, single submitterVCV000827509
91.
GRCh37:
Chr10:89623406
GRCh38:
Chr10:87863649
PTENHereditary cancer-predisposing syndrome, not specifiedUncertain significance
(May 16, 2018)
criteria provided, multiple submitters, no conflictsVCV000419309
92.
GRCh37:
Chr10:89623408
GRCh38:
Chr10:87863651
PTENnot providedUncertain significance
(Jul 13, 2016)
criteria provided, single submitterVCV000488741
93.
GRCh37:
Chr10:89623412
GRCh38:
Chr10:87863655
PTENnot providedUncertain significance
(Jul 26, 2016)
criteria provided, single submitterVCV000488775
94.
GRCh37:
Chr10:89623413
GRCh38:
Chr10:87863656
PTENnot providedUncertain significance
(Dec 23, 2015)
criteria provided, single submitterVCV000234712
95.
GRCh37:
Chr10:89623415
GRCh38:
Chr10:87863658
PTENnot providedUncertain significance
(Apr 17, 2015)
criteria provided, single submitterVCV000488758
96.
GRCh37:
Chr10:89623421
GRCh38:
Chr10:87863664
PTENnot providedUncertain significance
(Feb 13, 2018)
criteria provided, single submitterVCV000488781
97.
GRCh37:
Chr10:89623425
GRCh38:
Chr10:87863668
PTENnot specified, PTEN hamartoma tumor syndromeConflicting interpretations of pathogenicity
(May 28, 2019)
criteria provided, conflicting interpretationsVCV000234695
98.
GRCh37:
Chr10:89623428
GRCh38:
Chr10:87863671
PTENPTEN hamartoma tumor syndrome, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Apr 6, 2018)
reviewed by expert panel
FDA Recognized Database
VCV000127674
99.
GRCh37:
Chr10:89623429
GRCh38:
Chr10:87863672
PTENnot providedUncertain significance
(Apr 10, 2018)
criteria provided, multiple submitters, no conflictsVCV000234403
100.
GRCh37:
Chr10:89623430
GRCh38:
Chr10:87863673
PTENnot providedUncertain significance
(Jun 8, 2016)
criteria provided, single submitterVCV000189498
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