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Items: 1 to 100 of 9250

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129933242, LOC129933243
+1631 more
Copy number gain
See cases
GPathogenic
LOC129934199, LOC129934200
+2457 more
Copy number gain
See cases
GBenign
ABCG5, ABCG8
+443 more
Copy number gain
See cases
GPathogenic
LOC129933677, LOC129933678
+104 more
Copy number gain
See cases
GUncertain significance
BCYRN1, CALM2
+94 more
Copy number loss
See cases
GPathogenic
BCYRN1, CALM2
+60 more
Copy number gain
See cases
GLikely pathogenic
EPCAM, KCNK12
+19 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
LOC129933700, LOC129933701
+9 more
Copy number loss
See cases
GPathogenic
LOC129933705, LOC129933706
+3 more
Deletion
Lynch syndrome
GPathogenic
LOC129933707, LOC129933708
+3 more
Deletion
Lynch syndrome
GPathogenic
MSH6
Single nucleotide variant
Lynch syndrome
GBenign
LOC129933706, MSH6
Single nucleotide variant
Lynch syndrome
GBenign
LOC129933706, MSH6
Single nucleotide variant
not provided
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
not provided
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
Lynch syndrome
GBenign
LOC129933706, MSH6
Single nucleotide variant
Lynch syndrome
GBenign
LOC129933706, LOC129933707
+2 more
Duplication
Lynch syndrome
GUncertain significance
LOC129933707, MSH6
+1 more
Duplication
Lynch syndrome
GUncertain significance
LOC129933706, LOC129933707
+2 more
Deletion
Lynch syndrome
GPathogenic
LOC129933707, LOC129933708
+3 more
Deletion
Lynch syndrome
GPathogenic
LOC129933706, MSH6
Duplication
(genic upstream transcript variant)
Hereditary cancer-predisposing syndrome
GLikely pathogenic
LOC129933706, MSH6
Single nucleotide variant
Lynch syndrome 5
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome 5
GUncertain significance
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
GUncertain significance
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
GUncertain significance
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome 5
GUncertain significance
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
LOC129933706, MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Breast and/or ovarian cancer
+3 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+2 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(non-coding transcript variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
GLikely benign
MSH6
Duplication
(5 prime UTR variant)
not provided
+2 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+1 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
LOC129933707, MSH6
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933707, LOC129933708
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933707, LOC129933708
+1 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
LOC129933707, MSH6
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
LOC129933707, LOC129933708
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933707, LOC129933708
+1 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
MSH6-related condition
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GUncertain significance
LOC129933707, LOC129933708
+1 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
LOC129933707, LOC129933708
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933707, LOC129933708
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933708, LOC129933707
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933707, MSH6
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
MSH6
Single nucleotide variant
(5 prime UTR variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+4 more
GBenign/Likely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
(M1fs)
Deletion
(frameshift variant +2 more)
Hereditary cancer-predisposing syndrome
GPathogenic
LOC129933707, MSH6
Deletion
not provided
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933708, LOC129933707
+1 more
Deletion
(splice donor variant +1 more)
Carcinoma of colon
GPathogenic
LOC129933707, LOC129933708
+1 more
Deletion
(splice donor variant +1 more)
not provided
GPathogenic
MSH6
Single nucleotide variant
(5 prime UTR variant +2 more)
MSH6-related condition
+5 more
GConflicting classifications of pathogenicity
MSH6
Indel
(initiator_codon_variant +1 more)
Hereditary cancer-predisposing syndrome
GPathogenic
MSH6
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
LOC129933707, LOC129933708
+1 more
Deletion
Lynch syndrome
GPathogenic
MSH6
(M1V)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
MSH6
(M1T)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
GLikely pathogenic
MSH6
(M1I)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
GPathogenic
MSH6
(M1fs)
Deletion
(frameshift variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GConflicting classifications of pathogenicity
MSH6
(M1I)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GLikely pathogenic
MSH6
(S2L)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +3 more)
Hereditary nonpolyposis colorectal neoplasms
GLikely benign
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