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Items: 1 to 20 of 21

1.

nsv4456473

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPDR1
,
NME8
,
GPR141BP
,
SFRP4
Location information:
Clinical significance:
Uncertain significance
ID:
49622108
variant
2.

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
3.

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
4.

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
5.

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
6.

nsv3912277

ID:
48475632
variant
8.

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
9.

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
10.

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
11.

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
12.

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
13.

nsv3899194

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BRWD1P3
,
TRGV10
,
LOC105375206
,
LOC100133177
,
TRG-AS1
,
GTF3C6P3
,
LOC105375183
,
LOC107986787
,
CDC14BL
,
LOC401324
,
GTF2IP13
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48462549
variant
14.

nsv3917263

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4649
,
LOC107986794
,
GLI3
,
LOC105375236
,
NIPSNAP2
,
VN1R26P
,
RWDD4P2
,
TUBG1P
,
RN7SL496P
,
PGAM2
,
LOC105375284
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480618
variant
15.

nsv3898448

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
INMT
,
LOC105375237
,
PPP1R14BP4
,
LOC101928618
,
NT5C3A
,
LOC105375220
,
RNU6-1085P
,
LOC100422519
,
LOC107986735
,
GARS1-DT
,
S100A11P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461803
variant
17.

nsv6315223

Variant type:
complex substitution
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AOC1
,
ACHE
,
ACTB
,
ADCY1
,
ADCYAP1R1
,
AEBP1
,
AHR
,
AKR1B1
,
AMPH
,
AOAH
,
AQP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680170
variant
18.

nsv4352523

Variant type:
inversion
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACHE
,
ADCY1
,
ADCYAP1R1
,
AEBP1
,
AMPH
,
AOAH
,
AQP1
,
ASL
,
ASNS
,
AZGP1
,
BLVRA
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49347436
variant
19.

nsv6313670

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADCYAP1R1
,
AMPH
,
AOAH
,
AQP1
,
SEPTIN7
,
CHN2
,
CRHR2
,
GARS1
,
GHRHR
,
PDE1C
,
RP9
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
53677541
variant
20.

nsv6634332

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RRBP1P1
,
SLC29A4P1
,
PDGFA-DT
,
GTPBP10
,
ATG9B
,
OR9P1P
,
OR2A5
,
ABCA13
,
POU6F2-AS2
,
PMS2P11
,
SHH
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54348635
variant
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