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Items: 15

1.

nsv3902883

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC440181
,
HEATR5A-DT
,
SETP1
,
LOC105370640
,
RNU6-366P
,
LRR1
,
LOC105370534
,
IGHV2-5
,
TRP-TGG1-1
,
IGHVIII-5-1
,
PTPN21
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466238
variant
2.

nsv3907460

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BANF1P1
,
IGHV1-68
,
IGHD6-6
,
VESTAR
,
MIR4506
,
LINC00221
,
MIR494
,
ENTPD5
,
TRAJ55
,
IGHVII-65-1
,
BAZ1A-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470815
variant
3.

nsv3899639

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100289511
,
RNU6-552P
,
AKT1
,
LOC105370473
,
TRAJ38
,
RNU6-1239P
,
IGHD2-21
,
KRT18P7
,
RN7SKP255
,
SNORD114-15
,
CBLN3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48462994
variant
4.

nsv3903256

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DHRS7
,
MIR548Y
,
TRL-TAG4-1
,
IGHD1-7
,
SNORD114-4
,
LOC105370583
,
YLPM1
,
SNAPC1
,
NCOA4P1
,
PSME2
,
PRPF39
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466611
variant
5.

nsv3919106

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SRMP2
,
IGHV3-71
,
TRP-AGG2-5
,
RNU6-419P
,
BTBD7
,
IGHV6-1
,
MYH6
,
COQ6
,
TRAJ26
,
RPL22P2
,
TRDV2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482461
variant
6.

nsv3904265

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CRIP1
,
GPATCH2L
,
SNORD113-8
,
RPL7AP3
,
MIR4504
,
OR11H5P
,
RNU1-47P
,
PCNX4
,
LOC107984663
,
LOC105370660
,
RN7SKP21
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467620
variant
7.

nsv3917422

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR656
,
TRAJ59
,
BANF1P1
,
OR11H6
,
LINC02317
,
FOXG1
,
LOC107984670
,
RPL3P3
,
FAM181A
,
RNU6ATAC30P
,
RPS6P24
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480777
variant
8.

nsv6315524

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PAPOLA-DT
,
LOC105378180
,
NANOGP7
,
IGHV1-17
,
RPS8P1
,
LOC105370546
,
MIR485
,
GCATP1
,
CCDC88C
,
SLC25A29
,
KCNK13
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680471
variant
10.

nsv5980451

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACTN1
,
ACYP1
,
PARP1P2
,
ARG2
,
ZFP36L1
,
ENTPD5
,
CDKN3
,
DLST
,
EIF2S1
,
ERH
,
ESR2
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
52885802
variant
11.

nsv5380972

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL21P9
,
LOC100419668
,
PIGH
,
CCDC196
,
VTI1B
,
EIF1AXP2
,
LINC02290
,
MIR5694
,
NCOA4P1
,
FUT8
,
RAD51B
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
51636229
variant
12.

nsv4675709

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RDH11
,
RN7SL369P
,
LOC100421541
,
PLEKHH1
,
ATP6V1D
,
ARG2
,
COX7A2P1
,
TMEM229B
,
LOC100419668
,
HMGB1P34
,
PALS1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50272534
variant
13.

nsv6314209

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLEK2
,
EIF2S1
,
RNA5SP386
,
PALS1
,
HMGB1P34
,
PIGH
,
LOC100419668
,
MIR5694
,
VTI1B
,
SF3B4P1
,
GPHN
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53678080
variant
14.

nsv4675260

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLEKHH1
,
RDH11
,
ARG2
,
COX7A2P1
,
RNA5SP386
,
RN7SL213P
,
RN7SL369P
,
LOC100421541
,
ZFYVE26
,
RDH12
,
RPL21P9
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50272085
variant
15.

nsv4436741

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL213P
,
RNA5SP386
,
ARG2
,
COX7A2P1
,
RDH12
,
ZFYVE26
,
VTI1B
,
RPL21P9
,
RDH11
,
RN7SL369P
,
LOC100421541
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49580345
variant
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