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Items: 1 to 20 of 40

1.

nsv3897738

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NOC4L
,
DDX51
Location information:
Clinical significance:
Benign
ID:
48461093
variant
2.

nsv3906083

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DDX51
,
NOC4L
Location information:
Clinical significance:
Benign
ID:
48469438
variant
3.

nsv3893663

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DDX51
,
NOC4L
Location information:
Clinical significance:
Benign
ID:
48457018
variant
4.

nsv3896053

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DDX51
,
NOC4L
Location information:
Clinical significance:
Benign
ID:
48459408
variant
5.

nsv3893285

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NOC4L
,
DDX51
Location information:
Clinical significance:
Benign
ID:
48456640
variant
6.

nsv4456657

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107987169
,
DDX51
,
NOC4L
,
EP400
,
EP400P1
Location information:
Clinical significance:
Uncertain significance
ID:
49622292
variant
7.

nsv4456242

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NOC4L
,
LOC107987169
,
EP400
,
EP400P1
,
DDX51
Location information:
Clinical significance:
Uncertain significance
ID:
49621877
variant
9.

nsv3904242

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP369
,
ST13P22
,
LOC101929432
,
CD63-AS1
,
NCKAP5L
,
RPS20P31
,
LINC02370
,
RNU6-1188P
,
LOC107984486
,
LOC100420442
,
OR6C2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467597
variant
10.

nsv3905447

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOH12CR2
,
OR8S21P
,
RPL21P103
,
LOC105369755
,
SETD1B
,
RNU6-600P
,
LOC105369649
,
NPFF
,
P2RX4
,
MON2
,
LETMD1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468802
variant
11.

nsv3897722

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4ATAC16P
,
PIGAP1
,
RPL21P18
,
RPL41
,
LOC105369976
,
LOC100421618
,
OAS3
,
LINC02417
,
IQSEC3-AS2
,
SLCO1B1
,
DSTNP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461077
variant
12.

nsv3914194

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BTG1P1
,
LOC105370073
,
NRIP2
,
GLTP
,
SMIM10L1
,
RILPL2
,
ANKRD52
,
RPL21P103
,
LOC105369649
,
TMEM119
,
RPL13AP22
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477549
variant
13.

nsv3904719

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR5BT1P
,
RECQL
,
CFAP73
,
A2ML1
,
NENFP2
,
BCAT1
,
SIRT4
,
RPL18P9
,
CCNT1
,
GPD1
,
RNA5SP373
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468074
variant
14.

nsv3913894

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TAOK3
,
LINC02405
,
LOC105370086
,
LOC100419701
,
PUS1
,
LOC105370012
,
RPLP0
,
CCDC92
,
ADGRD1
,
LINC02985
,
SNORA49
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477249
variant
15.

nsv3924220

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370080
,
LINC02985
,
MED13L
,
CCDC92
,
ADGRD1
,
LOC100287653
,
HCAR2
,
POP5
,
RPL36P15
,
COQ5
,
RPS6P21
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487575
variant
16.

nsv3920557

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMED2
,
GCN1
,
TMEM132C
,
CCDC60
,
LOC105370076
,
TCTN2
,
LOC107984445
,
SRRM4
,
VPS33A
,
LOC107984448
,
RPS11P5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483912
variant
17.

nsv3896575

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984448
,
LOC105370082
,
MORN3
,
NLRP9P1
,
TMEM132C
,
TCTN2
,
GCN1
,
LOC105370076
,
SBNO1-AS1
,
RPS20P30
,
TRA-TGC3-2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459930
variant
18.

nsv3923347

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370044
,
RNU6-1017P
,
LOC105370041
,
ATP6V0A2
,
KDM2B
,
CCDC150P1
,
LOC105370061
,
SETD1B
,
LOC105370087
,
XLOC_009911
,
LOC105379613
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486702
variant
19.

nsv3921145

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF268
,
PTP4A1P2
,
RNA5SP378
,
LOC101928416
,
NOC4L
,
LOC100419935
,
PGBD3P3
,
ADGRD1
,
PUS1
,
LINC02824
,
CCDC92
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484500
variant
20.

nsv3911281

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMEM132C
,
RPL23AP67
,
RPL22P19
,
LINC02347
,
LOC105370073
,
LOC105370076
,
RPS20P30
,
LINC02393
,
RFLNA
,
ZNF10
,
TCTN2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474636
variant
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