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Links from Gene

Items: 32

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM72D
(N113S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACP6, ADAM15
+293 more
Copy number gain
Chromosome 1q21.1 duplication syndrome
GPathogenic
FAM72D
(I72V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM72D
(L25F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM72D
(Y60C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM72D
(F101L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
FAM72D
(D46N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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, ADAMTSL4
+103 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+43 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number loss
See cases
GLikely pathogenic
ACP6, ANKRD34A
+178 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number loss
See cases
GPathogenic
FAM72D, PPIAL4G
+1 more
Copy number gain
See cases
GLikely benign
LOC129931352, LOC129931353
+183 more
Copy number loss
See cases
GPathogenic
LOC126805853, LOC126805854
+153 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+179 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+178 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+35 more
Copy number gain
See cases
GPathogenic
FAM72D, PPIAL4G
+1 more
Copy number gain
See cases
GLikely benign
FAM72D, PPIAL4G
Copy number loss
See cases
GBenign
ACP6, ANKRD34A
+39 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+37 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+24 more
Copy number gain
See cases
GUncertain significance
ACP6, ANKRD34A
+153 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number gain
See cases
GPathogenic
LOC126805854, LOC128071544
+179 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+168 more
Copy number gain
See cases
GPathogenic
BCL9, LINC00623
+213 more
Copy number gain
See cases
GPathogenic
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