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Items: 15

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
3.

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
4.

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
5.

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
6.

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.

nsv3902272

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACTN3
,
GRK2
,
ARL2
,
BBS1
,
VPS51
,
MRPL49
,
ZNHIT2
,
CAPN1
,
CFL1
,
CST6
,
CTSW
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48465627
variant
11.

nsv6290938

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCS
,
RN7SL12P
,
CCDC87
,
TRS-GCT3-1
,
RNU4-39P
,
CNIH2
,
ACTN3
,
CTSF
,
RIN1
,
RBM14-RBM4
,
RBM4B
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53636333
variant
12.

nsv7094093

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
B4GAT1
,
CHKA-DT
,
ALDH3B1
,
DOC2GP
,
CORO1B
,
B4GAT1-DT
,
RNU7-23P
,
UNC93B5
,
MIR6752
,
FOSL1
,
MIR4691
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55274282
variant
14.

nsv7093406

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRPL11
,
NPAS4
,
CCDC87
,
RNU4-39P
,
CCS
,
ACTN3
,
CTSF
,
RBM14-RBM4
,
DPP3-DT
,
DPP3
,
RBM4
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55267800
variant
15.

nsv6314012

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100505524
,
ZDHHC24
,
PELI3
,
DPP3
,
DPP3-DT
,
MRPL11
,
NPAS4
,
RBM14
,
BBS1
,
RBM14-RBM4
,
ACTN3
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53677883
variant
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