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Items: 1 to 20 of 27

1.

nsv6312421

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COG5
,
DUS4L-BCAP29
,
DUS4L
,
RPL37AP6
,
GPR22
Location information:
Clinical significance:
Pathogenic
ID:
53676292
variant
2.

nsv7097101

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COG5
,
DUS4L-BCAP29
,
DUS4L
Location information:
Clinical significance:
Pathogenic
ID:
55277290
variant
3.

nsv6312518

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COG5
,
DUS4L-BCAP29
,
DUS4L
Location information:
Clinical significance:
Pathogenic
ID:
53676389
variant
4.

nsv3887149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BCAP29
,
WBP1LP2
,
BANF1P5
,
DUS4L-BCAP29
Location information:
Clinical significance:
Likely benign
ID:
48450504
variant
5.

nsv3896814

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DUS4L-BCAP29
,
BCAP29
,
DUS4L
,
COG5
Location information:
Clinical significance:
Uncertain significance
ID:
48460169
variant
6.

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
7.

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
8.

nsv3924380

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102724434
,
LRRN3
,
DNAJB9
,
SNORA25B
,
RPL7P32
,
LOC100131785
,
LOC105375457
,
PIK3CG
,
MIPEPP1
,
ANKRD49P4
,
KMT2E-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487735
variant
9.

nsv6313576

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LHFPL3-AS2
,
CTB-30L5.1
,
LOC105375462
,
LOC105375445
,
EFCAB10
,
DLD
,
FIS1
,
SRPK2
,
RPL3P8
,
POLR2J2
,
LOC105375465
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677447
variant
10.

nsv4675322

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CBLL1-AS1
,
COMETT
,
MTND4P6
,
LSMEM1
,
LOC107986838
,
LOC100422456
,
DNAJB9
,
SMIM30
,
LYPLA1P1
,
LOC100420226
,
LRRN3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272147
variant
11.

nsv6313503

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GJC3
,
LAMB4
,
PVRIG2P
,
DUS4L-BCAP29
,
CBLL1-AS1
,
RN7SKP86
,
MIR4467
,
EIF4BP6
,
LOC107986835
,
CYP3A43
,
RELN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677374
variant
12.

nsv3912378

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DNAJC2
,
LOC100420226
,
LOC100289561
,
RNU6-1136P
,
DNAJB9
,
RPL19P12
,
LRRN3
,
PIK3CG
,
MIR4467
,
LOC105375446
,
RPL23AP95
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475733
variant
15.

nsv4578664

ID:
50058414
variant
16.

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
17.

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
18.

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
19.

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
20.

nsv3922815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEPTIN7P6
,
MIR93
,
TAS2R4
,
RNA5SP247
,
RNU6-393P
,
LOC105375505
,
TRBV12-3
,
LOC107986829
,
CPSF4
,
GCC1
,
LOC349160
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486170
variant
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