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Items: 61

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LINC00685, LOC101929148
+160 more
Duplication
Autism
GLikely pathogenic
AKAP17A, AMELY
+88 more
Copy number loss
See cases
GPathogenic
AKAP17A, AMELY
+101 more
Copy number loss
See cases
GPathogenic
AKAP17A, AMELY
+162 more
Copy number loss
See cases
GPathogenic
AKAP17A, AMELY
+162 more
Copy number loss
See cases
GPathogenic
AKAP17A, AMELY
+83 more
Copy number gain
See cases
GLikely pathogenic
AKAP17A, AMELY
+158 more
Copy number loss
See cases
GPathogenic
AMELY, BPY2
+129 more
Copy number loss
See cases
GPathogenic
FAM197Y7, FAM197Y8
+64 more
Copy number gain
See cases
GPathogenic
AMELY, DDX3Y
+54 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+124 more
Copy number gain
See cases
GPathogenic
TTTY3B, TTTY4
+124 more
Copy number loss
See cases
GPathogenic
FAM197Y5, FAM197Y6
+124 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+124 more
Copy number gain
See cases
GPathogenic
AMELY, CDY2A
+100 more
Copy number gain
See cases
GPathogenic
FAM197Y5, FAM197Y6
+100 more
Copy number gain
See cases
GPathogenic
TTTY2, TTTY20
+85 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+110 more
Copy number gain
See cases
GPathogenic
AMELY, CDY2A
+61 more
Copy number gain
See cases
GPathogenic
TMSB4Y, TSPY1
+112 more
Copy number loss
See cases
GPathogenic
AMELY, BPY2
+106 more
Copy number gain
See cases
GPathogenic
FAM197Y2, FAM197Y3
+12 more
Copy number gain
See cases
GLikely benign
AMELY, CDY2A
+42 more
Copy number gain
not provided
GPathogenic
FAM197Y1P, TSPY1
+17 more
Copy number loss
not provided
GUncertain significance
AMELY, FAM197Y1P
+32 more
Copy number loss
Klinefelter syndrome
GPathogenic
TTTY8B, TTTY9A
+82 more
Copy number gain
Global developmental delay
GPathogenic
PRORY, PRY
+81 more
Copy number loss
not provided
GPathogenic
TSPY1, TSPY10
+3 more
Copy number loss
not provided
GUncertain significance
TSPY4, TSPY3
+1 more
Copy number loss
not provided
GLikely benign
TSPY4, TTTY20
+4 more
Copy number gain
not provided
GLikely benign
AMELY, BPY2
+81 more
Copy number gain
not provided
GPathogenic
AMELY, DDX3Y
+38 more
Copy number gain
not provided
GPathogenic
AMELY, DDX3Y
+36 more
Copy number gain
not provided
GPathogenic
AMELY, CDY2A
+42 more
Copy number gain
not provided
GPathogenic
AMELY, CDY2A
+42 more
Copy number gain
not provided
GPathogenic
AMELY, DDX3Y
+41 more
Copy number gain
not provided
GPathogenic
AMELY, DDX3Y
+41 more
Copy number gain
not provided
GPathogenic
TMSB4Y, TSPY1
+62 more
Copy number gain
not provided
GPathogenic
AMELY, CDY2A
+58 more
Copy number gain
not provided
GPathogenic
AMELY, FAM197Y1P
+33 more
Copy number gain
not provided
GPathogenic
AMELY, DDX3Y
+36 more
Copy number loss
not provided
GPathogenic
TSPY1, TSPY10
+4 more
Copy number loss
not provided
GUncertain significance
TSPY10, TSPY2
+81 more
Copy number loss
See cases
GPathogenic
AMELY, BPY2
+81 more
Copy number gain
See cases
GUncertain significance
AMELY, BPY2
+81 more
Copy number gain
See cases
GUncertain significance
AMELY, FAM197Y9
+14 more
Copy number gain
See cases
GLikely benign
AMELY, BPY2
+81 more
Copy number loss
See cases
GPathogenic
AMELY, BPY2
+82 more
Copy number loss
See cases
GPathogenic
AMELY, BPY2
+82 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+82 more
Copy number loss
See cases
GPathogenic
AMELY, BPY2
+82 more
Copy number gain
See cases
GPathogenic
AMELY, DDX3Y
+38 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+81 more
Copy number gain
See cases
GPathogenic
RBMY1J, RPS4Y1
+82 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+82 more
Copy number gain
See cases
GPathogenic
TSPY3, TSPY4
+82 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+81 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+81 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+81 more
Copy number loss
See cases
GPathogenic
DAZ3, DAZ4
+81 more
Copy number gain
See cases
GPathogenic
AMELY, BPY2
+81 more
Copy number gain
See cases
GPathogenic
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