U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 28

2.

nsv3873978

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100422029
,
H2AZ1
,
LOC101928217
,
LINC02435
,
RHOH
,
RNU6-35P
,
DCK
,
CEP44
,
LOC105378242
,
RN7SL492P
,
LOC105374392
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437333
variant
3.

nsv3876533

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100420289
,
LOC100131038
,
HS3ST1
,
UGDH
,
MTATP6P9
,
LOC105377495
,
RNU6-310P
,
TBCK
,
AGA-DT
,
MYL5
,
LOC105377604
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439888
variant
4.

nsv3884499

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND4LP29
,
RNU6-128P
,
LINC01258
,
LOC101927179
,
LINC02173
,
CTBP1-AS
,
GALNT7-DT
,
LOC391711
,
TBC1D1
,
SUMO2P11
,
RN7SKP235
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447854
variant
5.

nsv3880085

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268460
,
LINC02435
,
MIR576
,
RN7SL492P
,
PRMT5P1
,
DEFB108F
,
LOC100422029
,
USP17L24
,
LINC00575
,
TAPT1
,
LINC02503
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443440
variant
6.

nsv3883791

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377343
,
PDGFC
,
LOC105374535
,
RPL7AP29
,
LOC101928893
,
GATB
,
LOC102723704
,
LOC101928658
,
LOC105377558
,
NAAA
,
LOC107986328
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447146
variant
7.

nsv3875534

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KLKB1
,
NDST3
,
LOC112268472
,
NDST4
,
MTND3P3
,
ZGRF1
,
LSM6
,
PRSS48
,
LOC100287014
,
RNU6-1217P
,
TENM3-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438889
variant
8.

nsv3874596

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL6P12
,
F11
,
GK3
,
TENM3-AS2
,
LRBA
,
ING2-DT
,
GPM6A-DT
,
LOC107986192
,
KLKB1
,
LOC100287014
,
TLL1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437951
variant
9.

nsv3924008

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PPID
,
METTL14-DT
,
RNU6-335P
,
LOC729218
,
LINC02492
,
ABCE1
,
LINC02355
,
LINC02174
,
RN7SL776P
,
LOC729870
,
POU4F2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487363
variant
10.

nsv3874610

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OTUD4
,
LOC105377590
,
ACSL1
,
RNU6-1054P
,
LOC107986237
,
RNU6-1230P
,
FLJ38576
,
LINC02269
,
ARHGAP10
,
SNORD73A
,
UCP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437965
variant
11.

nsv3918110

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SCRG1
,
KRT18P51
,
LOC107986315
,
PHB1P14
,
LINC02436
,
RN7SL205P
,
LOC105377436
,
YWHAQP4
,
AADAT
,
RPL7AP27
,
RNA5SP168
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481465
variant
12.

nsv4455301

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SMARCA5
,
SFRP2
,
KLHL2
,
RN7SL253P
,
MORF4
,
LOC105377582
,
RNU6ATAC13P
,
LOC105377476
,
LOC152594
,
LINC01099
,
LOC105377508
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49620936
variant
13.

nsv3911855

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL26P16
,
LOC105377506
,
LOC105377509
,
TNRC18P1
,
LOC105377423
,
LOC105377529
,
GALNTL6-AS1
,
RNU6-506P
,
PCDH18
,
LOC107986314
,
CBR4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475210
variant
14.

nsv3911177

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNORD73B
,
CENPU
,
LINC01262
,
LOC101928052
,
LOC105377505
,
LOC105377611
,
MAML3
,
LOC105377588
,
IQCM
,
DBET
,
HHIP-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474532
variant
15.

nsv3914528

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATP5MGP4
,
LOC391710
,
LOC391713
,
LOC105377534
,
ASS1P8
,
LOC102724785
,
LOC107986239
,
LINC02362
,
TARS2P1
,
LINC01596
,
USP38
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477883
variant
16.

nsv3922745

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMEM131L
,
MTCO1P9
,
POU4F2
,
LOC107986238
,
ANP32CP
,
CLCN3
,
NUDT19P5
,
RNU6-335P
,
SAP30
,
LOC105377485
,
PALLD
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486100
variant
17.

nsv3871834

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377452
,
LOC105377558
,
RPL5P13
,
LOC101928131
,
LOC105377561
,
LOC105377475
,
NCOA4P3
,
SMAD1
,
MND1
,
GATB
,
RPPH1-3P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48435189
variant
18.

nsv3916456

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986328
,
MARK2P4
,
MIR3688-2
,
PALLD-AS1
,
GPM6A
,
LINC02374
,
RPL19P8
,
WWC2-AS2
,
LOC105377500
,
RNU6-1055P
,
GLRB
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479811
variant
19.

nsv3882398

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377519
,
CLDN22
,
LOC729558
,
LOC100129957
,
CCDC110
,
TMEM184C
,
NSA2P6
,
ING2-DT
,
GK3
,
SLC25A4
,
POU4F2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445753
variant
20.

nsv4457244

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377509
,
MIR3140
,
RNA5SP175
,
NMTRQ-TTG15-1
,
LINC02477
,
FAUP3
,
MTCO3P9
,
FHIP1A-DT
,
LINC02433
,
RNF175
,
LOC105377612
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49622879
variant
Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center