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Items: 1 to 20 of 52

1.

nsv3910581

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TPRX1P1
,
ZCCHC24
,
EIF5AL1
,
LOC729815
,
LOC105378383
Location information:
Clinical significance:
Uncertain significance
ID:
48473936
variant
2.

nsv4682723

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PPIF
,
ZMIZ1
,
EIF5AL1
,
ZCCHC24
,
TPRX1P1
,
SFTPA2
,
LOC729815
,
RPS12P18
,
LOC105378383
Location information:
Clinical significance:
Pathogenic
ID:
50285403
variant
3.

nsv7137209

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-12P
,
RNU1-65P
,
AGAP6
,
RPL15P13
,
LHPP
,
MTCO2P23
,
CHAT
,
LINC02935
,
XRCC6P1
,
MIR548F1
,
ENTPD1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55356054
variant
4.

nsv3913013

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS4XP17
,
SNORA67
,
RPA1
,
CTNS
,
CHRNE
,
ZZEF1
,
MIR3183
,
OR3A2
,
DERL2
,
POLR2A
,
GP1BA
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476368
variant
11.

nsv7098895

ID:
55279528
variant
12.

nsv4676022

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DVL2
,
PHF23
,
GPS2
,
RPL7AP64
,
ELP5
,
ACAP1
,
RNASEK
,
EIF5A
,
PLSCR3
,
MIR324
,
SLC16A11
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272847
variant
13.

nsv3922376

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DVL2
,
SPEM2
,
PHF23
,
TNK1
,
CLDN7
,
CHRNB1
,
ZBTB4
,
YBX2
,
ELP5
,
EIF5A
,
FGF11
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485731
variant
14.

nsv4729957

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR324
,
SLC2A4
,
KCTD11
,
GABARAP
,
DLG4
,
TMEM95
,
NEURL4
,
CTDNEP1
,
PHF23
,
DVL2
,
YBX2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50373594
variant
15.

nsv1398520

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EIF5A
,
ELP5
,
RPL7AP64
,
NEURL4
,
CTDNEP1
,
DVL2
,
PHF23
,
SLC2A4
,
MIR324
,
DLG4
,
GABARAP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
30348183
variant
16.

nsv1398446

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ASGR1
,
ACADVL
,
YBX2
,
PHF23
,
CLDN7
,
GABARAP
,
DLG4
,
DVL2
,
CTDNEP1
,
MIR324
,
SLC2A4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
30348109
variant
17.

nsv3906389

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100419870
,
LOC102724439
,
LOC105378313
,
ELOVL3
,
MIR936
,
YWHAZP5
,
RN7SL394P
,
LOC105376398
,
PWWP2B
,
MIR4675
,
DUSP8P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469744
variant
18.

nsv3891157

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AGAP14P
,
LOC100505502
,
LINC01514
,
LOC105378549
,
SIRT1
,
UROS
,
LOC105378443
,
KSR1P1
,
LOC105378314
,
LINC02663
,
LOC100130881
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454512
variant
19.

nsv3902271

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ANXA11
,
EDRF1-DT
,
TSPAN14
,
NUTM2A-AS1
,
LOC105378549
,
LINC02646
,
KCNMA1
,
RN7SKP196
,
LOC105376357
,
LOC105378552
,
GLRX3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465626
variant
20.

nsv3891958

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TUBB8
,
PPP2R2D
,
NRAP
,
LOC105376475
,
LOC101928834
,
LOC105376372
,
ITPRIP-AS1
,
LINC00702
,
LIPF
,
CASC2
,
RNU6-1090P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455313
variant
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