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Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
H3C13
(D124N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
(L110Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
(S88P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
(K80N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
(Q77L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
(R70Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
Single nucleotide variant
(synonymous variant)
not provided
GBenign
H3C13, LOC129931372
Single nucleotide variant
(synonymous variant)
not provided
GBenign
H3C13, LOC129931372
(P39L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C13, LOC129931372
(T23A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACP6, ADAM15
+263 more
Copy number gain
not specified
GPathogenic
ACP6, ADAM15
+315 more
Copy number gain
not specified
GPathogenic
ANP32E, APH1A
+25 more
Copy number loss
not specified
GPathogenic
ACP6, ADAM15
+293 more
Copy number gain
Chromosome 1q21.1 duplication syndrome
GPathogenic
FCGR3A, LCE3C
+956 more
Duplication
Parathyroid carcinoma
+2 more
GUncertain significance
CD34, CD46
+2014 more
Copy number gain
See cases
GPathogenic
GPATCH2, GPATCH3
+2014 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+42 more
Copy number gain
See cases
GLikely pathogenic
ACP6, ADAMTSL4
+103 more
Copy number gain
See cases
GPathogenic
CIART, LCE2A
+154 more
Copy number gain
Chromosome 1q21.1 duplication syndrome
GPathogenic
H2AC19, H2AC20
+15 more
Copy number gain
Breast ductal adenocarcinoma
GUncertain significance
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