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Items: 1 to 20 of 26

1.

nsv7095552

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ASXL1
Location information:
Clinical significance:
Pathogenic
ID:
55275741
variant
2.

nsv7096020

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ASXL1
Location information:
Clinical significance:
Pathogenic
ID:
55276209
variant
3.

nsv997038

Variant type:
copy number variation
Associated study:
nstd45
Organism:
human
Genes(s) in region:
ASXL1
Location information:
Clinical significance:
Pathogenic
ID:
17336680
variant
4.

nsv3891019

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NOL4L
,
ASXL1
Location information:
Clinical significance:
Likely pathogenic
ID:
48454374
variant
5.

nsv3918473

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NOL4L
,
ASXL1
Location information:
Clinical significance:
Uncertain significance
ID:
48481828
variant
6.

nsv3912723

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985448
,
LOC105372613
,
NECAB3
,
MIR6871
,
LOC105372593
,
LOC105372630
,
EIF6
,
EFCAB8
,
ZHX3
,
DLGAP4
,
LOC101927182
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476078
variant
7.

nsv3892750

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TGIF2-RAB5IF
,
LOC105372609
,
PGBD4P2
,
DUXAP7
,
SPINT3
,
C20orf144
,
ASIP
,
BMP7-AS1
,
TRPC4AP
,
SHLD1
,
MCM8-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456105
variant
8.

nsv3905072

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LRRN4
,
SNRPB
,
ABHD12
,
SCAND1
,
RPL21P3
,
TGM2
,
RPL37AP1
,
RPS15AP1
,
SCP2D1-AS1
,
TMEM74B
,
PREX1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468427
variant
9.

nsv3895314

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PKIG
,
LINC01523
,
KCNK15-AS1
,
NELFCD
,
PCED1A
,
FAM210B
,
LOC105372492
,
PROCR
,
RPSAP1
,
ANKEF1
,
SPINT4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458669
variant
10.

nsv3896520

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COMMD7
,
RNU7-6P
,
RPL36P1
,
TTLL9
,
LINC01428
,
CD93
,
PARAL1
,
LOC101929863
,
LOC105372655
,
LOC107984001
,
LOC100131496
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459875
variant
11.

nsv3920218

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR3646
,
NPEPL1
,
LSM14B
,
RNU6-147P
,
RNU6ATAC34P
,
PCIF1
,
SNTA1
,
LOC105376989
,
LOC107985402
,
LOC100289473
,
DLGAP4-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483573
variant
12.

nsv3910142

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DYNLRB1
,
LOC107985402
,
OTOR
,
MKKS
,
GLRXP1
,
LOC107987277
,
NANP
,
POFUT1
,
RPL12P3
,
LINC01431
,
RNU1-131P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473497
variant
13.

nsv3904899

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TTLL9
,
ABHD12
,
NXT1-AS1
,
PLAGL2
,
DTD1-AS1
,
VSX1
,
LOC102723636
,
LOC101926935
,
DUXAP7
,
NCOR1P1
,
RNA5SP480
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468254
variant
14.

nsv3878906

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF3B
,
GINS1
,
KIZ
,
LOC102723636
,
RPL12P12
,
LOC391239
,
LOC105379482
,
RPS19P1
,
SYNDIG1
,
RNU6-192P
,
CST5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48442261
variant
15.

nsv3918053

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MYH7B
,
PPP1R16B
,
KIF3B
,
RPS3P2
,
MLLT10P1
,
ACTL10
,
RNA5SP532
,
LOC149935
,
LOC101929698
,
DUSP15
,
HSPE1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481408
variant
16.

nsv6313956

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372586
,
RNU6-384P
,
PCMTD1P8
,
NOL4L
,
LOC102723618
,
DUX4L33
,
MIR663AHG
,
TSPY26P
,
BPIFA4P
,
CHMP4B
,
FDX1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677827
variant
17.

nsv4457806

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EFCAB8
,
C20orf203
,
NORAD
,
BPIFB6
,
RPL12P3
,
DNMT3B
,
RPS2P1
,
RPL31P3
,
COX7BP2
,
XPOTP1
,
SUN5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49623441
variant
20.

nsv3912259

ID:
48475614
variant
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