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Items: 1 to 20 of 28

1.

nsv7094461

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PRIMA1
Location information:
Clinical significance:
Uncertain significance
ID:
55274650
variant
2.

nsv3893892

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DICER1
,
SERPINA13P
,
GSC-DT
,
GPR68
,
LINC02279
,
RNU4-22P
,
LINC02328
,
LINC02330
,
MOAP1
,
RPL36AP4
,
SERPINA6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457247
variant
3.

nsv4675107

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SHLD2P2
,
RPL15P2
,
LOC105370644
,
CYB5AP3
,
ZC3H14
,
EFCAB11
,
CHGA
,
LINC01147
,
CALM1
,
KCNK13
,
LOC105370624
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271932
variant
7.

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
8.

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
9.

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
10.

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
11.

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
12.

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
13.

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
14.

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
15.

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
16.

nsv3922094

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370614
,
LOC105370617
,
IGHG1
,
ADIPOR1P2
,
PLD4
,
ATXN3
,
LINC02311
,
IFI27L1
,
RN7SL587P
,
LOC105370637
,
IGHV3-66
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485449
variant
17.

nsv3915681

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHV3-32
,
SNORD114-31
,
MIR655
,
RNU4-68P
,
SLC25A47
,
RPS24P3
,
CRIP1
,
RNU1-47P
,
HOMER2P2
,
IGHV3-64D
,
IGHV3-30-2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479036
variant
18.

nsv6637825

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CHGA
,
SNORD114-26
,
RPL13P6
,
CAP2P1
,
SNORD114-28
,
LOC105370698
,
DIO3OS
,
SPATA7
,
PEBP1P1
,
ATG2B
,
IGHV1-24
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54356654
variant
19.

nsv3914983

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHD5-5
,
EML5
,
LOC105370675
,
EIF5
,
SNORD114-7
,
TC2N
,
TCL6
,
MIR370
,
LINC03117
,
IFI27
,
PEBP1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478338
variant
20.

nsv3921292

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHVII-15-1
,
LINC03117
,
ASB2
,
MIR889
,
LOC105370669
,
MIR770
,
MEG8
,
IGHV3-16
,
IGHV3-11
,
MIR410
,
MEG9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484647
variant
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