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Items: 1 to 20 of 67

1.

nsv3897543

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EFR3A
,
HHLA1
,
KCNQ3
,
LOC107986976
,
OC90
Location information:
Clinical significance:
Benign
ID:
48460898
variant
2.

nsv6637812

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EFR3A
,
HHLA1
,
KCNQ3
,
LOC107986976
,
OC90
Location information:
Clinical significance:
Uncertain significance
ID:
54356641
variant
3.

nsv4456435

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EFR3A
,
HHLA1
,
KCNQ3
,
LOC107986976
,
OC90
Location information:
Clinical significance:
Uncertain significance
ID:
49622070
variant
4.

nsv3910787

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HHLA1
,
LOC107986976
,
KCNQ3
,
OC90
,
EFR3A
Location information:
Clinical significance:
Uncertain significance
ID:
48474142
variant
5.

nsv3909347

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OC90
,
EFR3A
,
LOC107986976
,
HHLA1
,
KCNQ3
Location information:
Clinical significance:
Uncertain significance
ID:
48472702
variant
6.

nsv6637224

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-37P
,
LOC100420215
,
LOC102723447
,
SQLE-DT
,
SNORD168
,
LOC112268031
,
RNU6-12P
,
RNA5SP277
,
CCAT1
,
LOC105375721
,
LOC101927588
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54356053
variant
7.

nsv4674996

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
POU5F1B
,
DNAJC8P3
,
MTRF1LP2
,
LOC105375754
,
MIR5194
,
RNU6-1255P
,
RNU1-35P
,
MYC
,
LOC107986905
,
HPYR1
,
LRATD2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271821
variant
8.

nsv3915490

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986906
,
MIR1208
,
MIR1207
,
TRAPPC9
,
DNAAF11
,
MIR30B
,
LOC105375783
,
RNU1-35P
,
LOC102723635
,
RNU6-144P
,
MIR30D
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478845
variant
9.

nsv4455511

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTSS1
,
PCAT2
,
LINC02964
,
LOC105375769
,
EFR3A
,
ARF1P3
,
LOC105375743
,
PRNCR1
,
RN7SKP206
,
RN7SKP155
,
MIR4662B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621146
variant
11.

nsv3915173

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL474P
,
UNC5D
,
VN1R45P
,
MIOXP1
,
VIRMA
,
PRDM14
,
LOC100996662
,
ZFAT-AS1
,
C1GALT1P3
,
LOC105375779
,
LOC105375933
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478528
variant
12.

nsv3901821

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBC1D31
,
LOC105375740
,
ESCO2
,
MIR6847
,
TNFRSF10C
,
RHOBTB2
,
ATP6V1G1P2
,
LOC105375637
,
MTND5P41
,
RNU6-144P
,
MAFA
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465176
variant
13.

nsv4349554

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929488
,
TEX15
,
LOC105375789
,
MTND4LP26
,
LOC105379384
,
DEFA1B
,
MIR1302-7
,
PTP4A3
,
LOC101927997
,
LINC02990
,
XKR6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344467
variant
14.

nsv3916777

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL5P22
,
ARHGEF10
,
LOC107986952
,
FAM90A6P
,
LOC105375692
,
EFR3A
,
RNF139
,
NCAPGP1
,
LY6S
,
ZNNT1
,
CYCSP22
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480132
variant
15.

nsv3898123

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SPAG1
,
LOC101927657
,
PPIAP84
,
BMP1
,
TUSC3
,
LOC100129098
,
RPL10P18
,
LOC105375873
,
SQLE-DT
,
LOC105375638
,
SIRLNT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461478
variant
16.

nsv3908608

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01617
,
PENK-AS1
,
RPS2P33
,
IMPDH1P6
,
LOC105375716
,
OR7E157P
,
TRE-CTC14-1
,
PBK
,
MROH4P
,
PDLIM2
,
SNORD65B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471963
variant
17.

nsv3893757

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375890
,
TRE-CTC14-1
,
TARDBPP4
,
CYP11B2
,
ZFPM2-AS1
,
IMPDH1P6
,
RNY4P5
,
MIR548H4
,
LOC105379228
,
TMEM68
,
RPS2P33
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457112
variant
18.

nsv3923310

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268023
,
RPL23AP96
,
RN7SL228P
,
RNA5SP272
,
LOC107986976
,
ADCY8
,
MIR6841
,
LOC100422614
,
LY6D
,
LOC105375630
,
RN7SL19P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486665
variant
19.

nsv3914307

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986897
,
NUGGC
,
TRF-GAA12-1
,
RN7SKP29
,
TMEM74
,
RAD54B
,
CCNE2
,
ATP6V1G1P2
,
RNU6ATAC8P
,
PPP2CB
,
LOC105375785
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477662
variant
20.

nsv3919282

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4662B
,
LOC101927845
,
PTCSC1
,
LOC105375723
,
RNU1-124P
,
LOC105375932
,
CEBPD
,
OSGIN2
,
EBF2
,
LOC107986938
,
PABPC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482637
variant
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