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Items: 1 to 20 of 86

1.

nsv3871942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCT7P2
,
LDHBP3
,
LINC02058
Location information:
Clinical significance:
Benign
ID:
48435297
variant
2.

nsv3910630

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DAZAP2P1
,
RPL36AP16
,
TRIM51JP
,
LOC105373608
,
LOC105373903
,
LOC105374690
,
C2orf81
,
LOC105377627
,
LOC105373714
,
C2orf78
,
ELF2P4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473985
variant
3.

nsv3889848

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MEGF10
,
LOC100128407
,
RPL36AP20
,
CSNK1A1
,
LOC105374695
,
RPL36AP21
,
RNU4-14P
,
LOC105374672
,
LOC105377715
,
CATSPER2P2
,
LOC101927046
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453203
variant
4.

nsv6634330

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYP1B1-AS1
,
LOC107985771
,
C2orf15
,
APPAT
,
LINC01799
,
PNO1
,
CENPO
,
LOC102724744
,
RN7SL470P
,
TRQ-TTG5-1
,
LOC105374831
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54348633
variant
5.

nsv3912840

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CRB1
,
STX6
,
RPS23P9
,
SLAMF1
,
CRTC2
,
RN7SL372P
,
IL6R
,
RNU6-693P
,
RPL35AP5
,
C1orf105
,
ATP8B2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476195
variant
6.

nsv3884357

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TXNDC15
,
PCDHAC1
,
ZMAT2
,
RNU6-482P
,
PCDHB3
,
NCOA4P4
,
LOC101927488
,
ZRSR2P1
,
MIR548P
,
PCDHGA3
,
APBB3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447712
variant
7.

nsv3915450

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MCTP1
,
LOC102467217
,
LINC02234
,
MTND5P10
,
RNU6-752P
,
MTND3P19
,
MTCYBP40
,
RPL28P3
,
LOC345571
,
LOC101927078
,
LOC100289569
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478805
variant
8.

nsv3916468

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105379149
,
LOC107986365
,
SNCAIP
,
LOC105379126
,
MTATP6P2
,
LOC105379083
,
MTCO1P24
,
DDX43P1
,
LOC345576
,
TICAM2-AS1
,
GRAMD2B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479823
variant
9.

nsv3924896

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986438
,
GGCTP1
,
RN7SKP122
,
MAN2A1
,
SNORD138
,
TMEM161B-DT
,
MTCO1P22
,
CTBP2P4
,
CHD1-DT
,
LOC101929380
,
RPS9P3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48488251
variant
10.

nsv3914008

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105379080
,
LOC105379100
,
SPATA9
,
SLCO6A1
,
ADGRV1
,
LOC105379077
,
LYSETP1
,
RNU1-140P
,
RIOK2
,
LOC105379074
,
LOC107986436
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477363
variant
11.

nsv3921368

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986438
,
MTCO1P22
,
ADGRV1
,
SPATA9
,
CHD1-DT
,
MTCO2P22
,
TMEM161B
,
GGCTP1
,
LOC105379082
,
ARRDC3
,
MEF2C
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484723
variant
12.

nsv3879974

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105379090
,
LNPEP
,
MTCO2P22
,
NIHCOLE
,
RPS9P3
,
LINC01340
,
LOC101930276
,
RNA5SP188
,
RNU6-524P
,
LOC105379096
,
CRLF3P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443329
variant
13.

nsv3891146

ID:
48454501
variant
18.

nsv3903429

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PDZK1
,
LOC105369140
,
RNVU1-2
,
LOC107985593
,
SSBL4P
,
RNVU1-18
,
LOC102723321
,
LINC01632
,
LOC105371215
,
ACP6
,
CH17-125A10.2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466784
variant
20.

nsv3892632

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC728989
,
MIR6077
,
TRNAV-CAC
,
LOC112268272
,
TRN-GTT12-1
,
PFN1P3
,
LIX1L
,
RNU1-153P
,
TRQ-CTG7-1
,
PPIAL4D
,
FAM72C
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455987
variant
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