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Items: 1 to 20 of 61

1.

nsv6638081

Variant type:
insertion
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNJ6
Location information:
Clinical significance:
Uncertain significance
ID:
54356910
variant
2.

nsv3923176

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COL18A1-AS2
,
RCAN1
,
C21orf91-OT1
,
KRTAP13-2
,
KRTAP19-9P
,
VN2R20P
,
CYCSP42
,
HSPA13
,
RNU6-772P
,
BACH1-IT2
,
KRTAP25-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486531
variant
3.

nsv3905423

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND5P1
,
RPL37P3
,
PRDM15
,
PLAC4
,
C21orf62-AS1
,
MIR6814
,
DYRK1A
,
ITSN1
,
LINC00649
,
SETD4
,
LRRC3-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468778
variant
4.

nsv3917693

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DPRXP5
,
MIR6724-1
,
ZNF299P
,
KRTAP22-1
,
TMPRSS15
,
CHODL-AS1
,
MIR4759
,
LOC105369299
,
LOC105372774
,
OLIG1
,
MTRES1P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481048
variant
5.

nsv3913105

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KRTAP10-12
,
LINC01678
,
BRWD1-AS2
,
RPS26P4
,
LINC00479
,
PDE9A-AS1
,
LOC105372836
,
WDR4
,
HSF2BP
,
LOC105372813
,
DNMT3L-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476460
variant
6.

nsv3908171

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AIRE
,
LSS
,
PSMG1
,
SNORA91
,
KCNJ6-AS1
,
KRTAP12-1
,
UMODL1
,
GET1-SH3BGR
,
MIR6070
,
MIR6815
,
NDUFV3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471526
variant
7.

nsv3908653

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR6070
,
KCNJ6-AS1
,
LOC105372839
,
LINC00205
,
SUMO3
,
BNAT1
,
PDE9A-AS1
,
LOC107985485
,
COL18A1
,
LSS
,
GATD3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472008
variant
8.

nsv3918954

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LCA5L
,
B3GALT5-AS1
,
DIP2A
,
FTCD
,
LINC02940
,
TFF1
,
PCNT
,
LINC01668
,
LOC105372826
,
C2CD2
,
RPL18AP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482309
variant
9.

nsv3891817

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985513
,
LOC101928398
,
LINC01700
,
TFF2
,
LOC105372804
,
TMPRSS3
,
SMIM34
,
LOC107987299
,
LOC101928269
,
LINC00310
,
RNA5SP491
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455172
variant
16.

nsv1398033

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100288590
,
DYRK1A
,
LOC105369305
,
KCNJ6
,
LOC107985492
,
LOC105369308
,
DSCR4
,
DSCR10
,
PIGP
,
LINC01423
,
HLCS
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
30347696
variant
17.

nsv4768385

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DYRK1A
,
LOC100288590
,
SNRPGP13
,
ETS2-AS1
,
LOC105372797
,
LOC101928368
,
LOC107985480
,
RPSAP64
,
LOC105372802
,
DSCR8
,
ERG
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50453190
variant
18.

nsv4768387

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNRPGP13
,
LOC105372797
,
ETS2-AS1
,
LOC101928368
,
LOC107985480
,
ERG
,
RPSAP64
,
KCNJ6-AS1
,
LOC105372802
,
DSCR8
,
LINC00114
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50453192
variant
19.

nsv1398119

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372797
,
KCNJ15
,
LOC107985513
,
LOC101928398
,
DSCR4
,
LOC105372801
,
LOC105372798
,
LINC00114
,
KCNJ6-AS1
,
SPATA20P1
,
DYRK1A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
30347782
variant
20.

nsv3910364

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372798
,
DYRK1A
,
LOC101928368
,
LOC105372797
,
LOC105372802
,
KCNJ6-AS1
,
ERG
,
DSCR8
,
LINC01423
,
KCNJ6
,
LOC107985513
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473719
variant
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