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Items: 1 to 20 of 24

1.

nsv6634311

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PDGFB
Location information:
Clinical significance:
Pathogenic
ID:
54348614
variant
2.

nsv4684334

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PDGFB
Location information:
Clinical significance:
Likely pathogenic
ID:
50287457
variant
3.

nsv3903513

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PDGFB
Location information:
Clinical significance:
Benign
ID:
48466868
variant
4.

nsv3902776

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100419811
,
MTCO2P20
,
SLC25A15P5
,
LOC101928824
,
POM121L9P
,
HSCB
,
LINC01644
,
MIRLET7BHG
,
C22orf42
,
CHKB-CPT1B
,
LOC105373024
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466131
variant
5.

nsv3894026

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGKV3OR22-2
,
ZDHHC8
,
IGLV3-16
,
LOC107985563
,
RPL39P41
,
TPST2
,
RPS17P16
,
IGLV3-12
,
BCR
,
TRIOBP
,
PES1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457381
variant
6.

nsv3890411

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-495P
,
KIAA1656
,
PLXNB2
,
LOC101927344
,
RASD2
,
WBP2NL
,
APOBEC3F
,
PITPNB
,
RN7SL268P
,
GGT1
,
LOC105372858
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453766
variant
7.

nsv4729926

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FBXO7
,
GTSE1
,
H1-0
,
RPL31P62
,
C22orf31
,
RNU6-28P
,
BCRP5
,
ESS2
,
SCUBE1
,
SBF1
,
RNA5SP494
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50373563
variant
8.

nsv3902598

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FABP5P11
,
SLC2A11
,
MIR301B
,
CHEK2P4
,
LOC107985567
,
RN7SKP80
,
ZMAT5
,
RPS10P31
,
LOC339666
,
IGLV4-3
,
TNFRSF13C
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465953
variant
9.

nsv3907231

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DDTL
,
PPP1R26P3
,
DENND6B
,
PATZ1
,
CNN2P1
,
LRRC37A14P
,
LOC112268295
,
MIR130B
,
LOC105369161
,
POM121L4P
,
GRAMD4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470586
variant
10.

nsv3890401

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
YPEL1
,
LINC02885
,
IGLV3-10
,
LOC105373069
,
KCTD17
,
IGLV3-15
,
IGLVVI-22-1
,
UQCR10
,
CCDC188BP
,
KRT18P5
,
TEF
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453756
variant
11.

nsv4457771

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGLV3-27
,
XKR3
,
ADSL
,
CCDC188BP
,
GAB4
,
NUP50-DT
,
LINC01664
,
NCF4-AS1
,
ANP32BP2
,
IGLV3-24
,
RN7SL6P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49623406
variant
12.

nsv3891895

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
POM121L7P
,
RPS10P31
,
IGLV3-30
,
MRPL40
,
LOC100131536
,
ZNF70
,
ACO2
,
MIR3928
,
MIR648
,
IGLV2-28
,
LOC107985573
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455250
variant
13.

nsv3913775

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF280A
,
RFPL1S
,
NCAPH2
,
IL17REL
,
MRTFA-AS1
,
SCUBE1-AS2
,
GAS2L1
,
RN7SL20P
,
ZDHHC8
,
KCNJ4
,
RTN4R
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477130
variant
14.

nsv3919881

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR12114
,
MIR6820
,
L3MBTL2-AS1
,
PI4KAP1
,
ZNF74
,
EIF3L
,
TSSK1A
,
PPP1R14BP1
,
LOC105373062
,
CYP2D6
,
RPL31P62
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483236
variant
15.

nsv3919085

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGLV2-28
,
LINC01310
,
MIR6818
,
TOP3BP1
,
IGLV2-14
,
CRYBA4
,
VPREB1
,
APOL2
,
SMTN
,
RPS29P31
,
LOC110091768
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482440
variant
16.

nsv4676292

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PDXP-DT
,
PDGFB
,
ACR
,
LOC105373037
,
TBC1D22A
,
LOC105373060
,
SEC14L2
,
APOL6
,
SYN3
,
LINC01656
,
CDC42EP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50273117
variant
17.

nsv3906962

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UQCRFS1P1
,
APOBEC3F
,
PLXNB2
,
LOC105373067
,
APOL2
,
RNU6-900P
,
LINC01310
,
LOC105373064
,
TNRC6B-DT
,
RNU6-379P
,
SLC25A17
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470317
variant
18.

nsv3910634

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HDAC10
,
RPS25P10
,
ST13
,
COX6B1P3
,
TTC38
,
CSDC2
,
RN7SKP210
,
LOC102724608
,
MGAT3-AS1
,
SERHL
,
SNORD43
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473989
variant
19.

nsv3910659

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100506472
,
MCHR1
,
PRR34
,
FAM118A
,
CYP2D8P
,
TRABD
,
MPPED1
,
LOC101927551
,
PARVB
,
RPL35P8
,
SNORD13P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474014
variant
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