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Items: 1 to 20 of 56

1.

nsv7093818

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CD3G
Location information:
Clinical significance:
Likely pathogenic
ID:
55274007
variant
2.

nsv6308963

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CD3D
,
CD3G
Location information:
Clinical significance:
Uncertain significance
ID:
53672834
variant
3.

nsv3919826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-438P
,
LOC105375300
,
URGCP
,
MOXD2P
,
LOC105375171
,
SP4
,
LOC105375194
,
LOC105375277
,
TRBV21-1
,
MIR4283-1
,
VN1R24P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483181
variant
4.

nsv3888815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986817
,
DNAJB9
,
LRRN3
,
SKAP2
,
LOC107986794
,
MAGI2-AS2
,
CPA2
,
MIR10525
,
VN1R37P
,
SPDYE7P
,
DPY19L1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452170
variant
5.

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
6.

nsv3897424

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986734
,
LINC00265
,
POLD2
,
SFRP4
,
MIR3943
,
MIR4649
,
LOC105375236
,
CFAP144P1
,
LOC105375250
,
TRG
,
TUBG1P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48460779
variant
7.

nsv3916442

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102724903
,
LINC01448
,
LINC00265
,
SFRP4
,
RPL36AP27
,
INHBA-AS1
,
POLD2
,
TRG
,
SNORA5B
,
LOC112267984
,
HUS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479797
variant
8.

nsv3912277

ID:
48475632
variant
9.

nsv3924742

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NUDCD3
,
KRT8P20
,
TRGVB
,
CDK13-DT
,
TRG-AS1
,
LOC105375252
,
MRPL32
,
TRGV10
,
LOC101928688
,
POLR2J4
,
TRGC2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48488097
variant
11.

nsv4683551

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR6716
,
TREHP1
,
DDX6
,
RPS25
,
CENATAC
,
IL10RA
,
RPL23AP64
,
TREH
,
RNU6-1157P
,
SMIM35
,
RPL5P30
,
See more...
Location information:
Clinical significance:
Uncertain significance,
Pathogenic
ID:
50286231
variant
12.

nsv3894780

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-565P
,
LAMB1
,
MIR5707
,
LOC100419774
,
ZNF786
,
ELK1P1
,
MTCYBP42
,
SSU72L6
,
EEF1A1P27
,
LOC105375200
,
THUMPD3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458135
variant
13.

nsv4455091

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP51
,
FLJ40288
,
STAG3L2
,
FKBP9
,
BNIP3P11
,
GPR37
,
LOC105375251
,
LOC100419642
,
LOC105375148
,
PMS2P7
,
TRBV10-3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49620726
variant
14.

nsv3909087

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MNX1-AS2
,
VN1R31P
,
PRSS58
,
LOC107986715
,
AHCYL2
,
BAIAP2L1
,
LOC107986821
,
NUPR2
,
SEPTIN7P4
,
PRKAR1B
,
TRBV15
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472442
variant
15.

nsv3908592

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRGV3
,
SNX10-AS1
,
LOC105375433
,
LOC101060796
,
OR9A2
,
LOC105375542
,
SPDYE2
,
NPY
,
RNU6-979P
,
RN7SL265P
,
RNY4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471947
variant
16.

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
17.

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
18.

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
19.

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
20.

nsv3915802

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP52
,
IQCE
,
LOC101928421
,
TRGJP2
,
CARD11
,
NUP42
,
FBXL18
,
TAX1BP1
,
RBAK-RBAKDN
,
LOC100533631
,
RPL26P21
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479157
variant
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