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Items: 14

1.

nsv5380796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FAUP4
,
MMP7
,
SETP17
,
LUZP2
,
MIR6124
,
KCTD9P4
,
CCND1
,
RNU6-1238P
,
RNA5SP339
,
MMP10
,
GPR152
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51636053
variant
2.

nsv3915804

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TPBGL
,
MAP6
,
THRSP
,
P2RY6
,
TSKU
,
MIR4692
,
LRRC32
,
TOMM20P1
,
LOC100419542
,
WNT11
,
PLEKHB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479159
variant
3.

nsv3916301

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL786P
,
LIPT2-AS1
,
XNDC1N
,
P2RY2
,
ATG16L2
,
ACER3
,
C2CD3
,
RNA5SP343
,
NUMA1
,
RN7SKP243
,
HNRNPA1P40
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479656
variant
5.

nsv3893233

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376598
,
OSBPL9P2
,
LOC100421985
,
NLRP10
,
GLB1L2
,
LINC02685
,
FTH1P16
,
PTS
,
SORL1-AS1
,
OR9G3P
,
OR8G5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456588
variant
6.

nsv3900144

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RTN3
,
KRTAP5-13P
,
LOC653503
,
LOC105376646
,
LOC105369539
,
MPPED2
,
DLG2
,
SORL1-AS1
,
YWHABP2
,
SCN3B
,
TRIM53AP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463499
variant
7.

nsv3908873

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHMBP2
,
SYTL2
,
LRRC32
,
RPS25
,
OR5AO1P
,
TREHP1
,
OR51A9P
,
CHRNA10
,
BATF2
,
GLYAT
,
PPP2R5B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472228
variant
8.

nsv6315537

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PYGM
,
ATL3
,
LOC105376656
,
LOC649133
,
RPL31P47
,
ALDH3B1
,
RNA5SP350
,
CATSPER1
,
MIR5582
,
MIR192
,
LOC105369571
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680484
variant
9.

nsv3898361

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SESN3
,
LOC107984352
,
AMOTL1
,
TRP-TGG2-1
,
LOC105369453
,
RPS3AP42
,
RN7SL786P
,
CASP12
,
ACER3
,
HIKESHI
,
LIPT2-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461716
variant
10.

nsv6314007

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
STARD10
,
PDE2A
,
RPS12P20
,
LOC105369376
,
FOLR3P1
,
LOC100421204
,
ART2P
,
LRTOMT
,
FOLR1P1
,
PDE2A-AS1
,
PHOX2A
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53677878
variant
11.

nsv7094183

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268078
,
LRTOMT
,
KRTAP5-10
,
OR2AT2P
,
LOC220077
,
LOC107984352
,
FOLR1P1
,
ART2P
,
STARD10
,
PDE2A-AS1
,
UNC93B6
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55274372
variant
12.

nsv3921153

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC220077
,
PHOX2A
,
KRTAP5-10
,
UNC93B6
,
KRTAP5-11
,
ALG1L9P
,
RNA5SP342
,
FOLR3P1
,
LAMTOR1
,
XNDC1N
,
DEFB131B
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48484508
variant
13.

nsv4681893

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E128P
,
ZNF705EP
,
KRTAP5-9
,
OR7E87P
,
KRTAP5-8
,
S100A11P3
,
NUMA1
,
DEFB131B
,
OR7E126P
,
RNA5SP342
,
XNDC1N
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50284573
variant
14.

nsv6637545

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLPB
,
FOLR3
,
LAMTOR1
,
RPEP6
,
LOC112268077
,
NUMA1
,
LOC401703
,
ANAPC15
,
INPPL1
,
MIR3165
,
PHOX2A
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54356374
variant
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