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Items: 1 to 20 of 25

1.

nsv3877822

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FASTKD1
,
LOC100421474
,
KLHL41
,
CFAP210
,
PPIG
Location information:
Clinical significance:
Benign
ID:
48441177
variant
2.

nsv3910630

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DAZAP2P1
,
RPL36AP16
,
TRIM51JP
,
LOC105373608
,
LOC105373903
,
LOC105374690
,
C2orf81
,
LOC105377627
,
LOC105373714
,
C2orf78
,
ELF2P4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473985
variant
3.

nsv4451512

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01117
,
LOC107985958
,
RNU7-44P
,
RPSAP25
,
RNU6-182P
,
MIR3606
,
DUSP19
,
IFT70B
,
MIR6512
,
PLEKHA3
,
CYB5AP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49617147
variant
4.

nsv4768307

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RBM45
,
LOC102724194
,
DLX1
,
TXNL4AP1
,
CHROMR
,
GCA
,
NSA2P5
,
EIF2S2P4
,
PRPS1P1
,
LOC105373757
,
RNU6-627P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50453112
variant
5.

nsv3904056

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PRKRA
,
STK39
,
XIRP2-AS1
,
LOC105373760
,
FUCA1P1
,
LOC105369143
,
PHF5AP5
,
PRPS1P1
,
CHROMR
,
RPS15AP14
,
KLHL41
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467411
variant
6.

nsv6315160

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EIF3EP3
,
FAP
,
DAP3P2
,
PHOSPHO2-KLHL23
,
KCNH7
,
UBE2V1P6
,
BAZ2B
,
LOC105373728
,
TTC21B
,
ALDH7A1P2
,
LOC107985959
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53679670
variant
7.

nsv3909452

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985959
,
TTC21B
,
LINC01305
,
SP9
,
GPR155-DT
,
PHOSPHO2-KLHL23
,
CHN1
,
DAP3P2
,
UBE2V1P6
,
KLHL23
,
LOC105373745
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472807
variant
10.

nsv6315390

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268439
,
RNA5SP116
,
FAP
,
EIF3EP3
,
LOC107985821
,
LOC105373602
,
SLC44A3P1
,
LOC100420775
,
LOC100506405
,
RGPD6
,
FAR2P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680337
variant
11.

nsv3874648

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGKV2OR2-10
,
LOC105374848
,
RN7SL313P
,
MIR3131
,
LOC107985957
,
RN7SKP179
,
EPCAM
,
RNU6-282P
,
LOC102723825
,
BOK
,
CD8B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438003
variant
12.

nsv3885544

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-674P
,
KANSL3
,
KHK
,
TM4SF20
,
ABCB11
,
BAZ2B-AS1
,
LOC105373506
,
ELOCP21
,
LOC105373612
,
LOC107985854
,
LOC107985960
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448899
variant
13.

nsv3882615

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND2P22
,
LOC112268410
,
ASIC4
,
LOC107985792
,
HAAO
,
RPL28P2
,
TRE-CTC7-1
,
RNU6-915P
,
CCDC138
,
LOC107986001
,
IGKV3D-7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445970
variant
14.

nsv4674383

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNORA41
,
LOC101929633
,
RPL17P10
,
SNORD51
,
LOC100507443
,
MIR548AE1
,
LOC101927741
,
LRP2
,
SCYL2P1
,
ZNF385B
,
B3GALT1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271208
variant
15.

nsv3876037

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01953
,
CTLA4
,
ABI2
,
MTCO1P17
,
GAPDHP59
,
GCSHP3
,
LOC107985785
,
SUMO1
,
BBS5
,
MIR1302-4
,
PPIAP68
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439392
variant
16.

nsv3875392

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR10B
,
SCN7A
,
PLA2R1
,
MIR6888
,
LINC01876
,
LOC102724058
,
RAPGEF4-AS1
,
RPL30P2
,
SCN2A
,
CYB5AP2
,
TRA-CGC3-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438747
variant
17.

nsv3874278

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985957
,
LOC101927073
,
LOC105373715
,
LOC105369143
,
CYP2C56P
,
LOC105373712
,
LOC105373709
,
HOXD11
,
PTP4A1P1
,
PPIAP66
,
TANC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437633
variant
18.

nsv3893853

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SCN7A
,
HEBP2P1
,
SCN9A
,
LOC107985958
,
LOC105373742
,
DLX2-DT
,
LOC100420002
,
RNU6-182P
,
GPD2
,
COBLL1
,
RNA5SP107
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457208
variant
19.

nsv1398397

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LRP2
,
SSB
,
ABCB11
,
B3GALT1
,
PPIG
,
DHRS9
,
KLHL41
,
STK39
,
METTL5
,
SPC25
,
G6PC2
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
30348060
variant
20.

nsv3880118

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYB5AP2
,
PTCHD3P2
,
METTL5
,
KLHL23
,
SNORD3K
,
BBS5
,
KLHL41
,
PPIG
,
FASTKD1
,
LOC171417
,
PHOSPHO2-KLHL23
,
See more...
Location information:
Clinical significance:
Benign
ID:
48443473
variant
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