U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 36

1.

nsv3914561

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR889
,
GLRX5
,
RPSAP5
,
MIR5195
,
RPL13P6
,
CLBA1
,
CRIP2
,
IGHVII-43-1
,
LOC105370661
,
MIR1185-1
,
BDKRB2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477916
variant
2.

nsv4684265

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB3P4
,
LINC02320
,
PACS2
,
EXOC3L4
,
SNORD114-29
,
MIR8071-1
,
IGHV3-50
,
BEGAIN
,
MIR433
,
LOC105370656
,
MTA1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50287388
variant
3.

nsv3911746

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR1185-2
,
LOC105370685
,
RPS26P49
,
IGHV3-30
,
TEX22
,
MIR2392
,
SNORD114-15
,
RPL21P13
,
IGHJ1P
,
MIR377
,
RAP2CP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475101
variant
4.

nsv3921506

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL21P13
,
EXOC3L4
,
SNORD114-29
,
MIR8071-2
,
SNORD113-7
,
MIR889
,
IGHV3-65
,
BEGAIN
,
MIR134
,
SNORD114-12
,
IGHV3-62
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484861
variant
5.

nsv3902723

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB3P4
,
TDRD9
,
COA8
,
BEGAIN
,
LOC105370673
,
LINC02298
,
INF2
,
CEND1P1
,
PACS2
,
SNORD114-12
,
LINC02320
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466078
variant
6.

nsv6291768

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC85C
,
MEG3
,
SNORD114-27
,
SNORD113-5
,
MIR323A
,
MIR758
,
HMGN1P25
,
MIR654
,
LOC100128373
,
C14orf132
,
MIR543
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53637163
variant
7.

nsv3920123

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR1193
,
SNORD114-19
,
SLC25A29
,
SNORD114-22
,
SNORD114-1
,
MIR412
,
SNORD114-4
,
MIR485
,
WARS1
,
MIR495
,
MIR409
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483478
variant
8.

nsv3924299

ID:
48487654
variant
11.

nsv4675243

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SKP92
,
MIR345
,
EML1
,
SLC25A47
,
YY1
,
LOC105370664
,
RNU1-47P
,
MIR151B
,
VDAC3P1
,
WARS1
,
RN7SL523P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272068
variant
12.

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
13.

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
14.

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
15.

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
16.

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
17.

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
18.

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
19.

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
20.

nsv3898512

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MEG3
,
IGHV7-27
,
GPR68
,
KIF26A
,
SNORD114-25
,
LOC101928352
,
LOC105370608
,
LINC02330
,
AHSA1
,
CCDC85C
,
MIR4309
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461867
variant
Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center