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Items: 1 to 20 of 144

1.

nsv4457065

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BRD9
,
TRIP13
,
ZDHHC11
Location information:
Clinical significance:
Uncertain significance
ID:
49622700
variant
2.

nsv3914649

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374666
,
CCNB3P1
,
BASP1-AS1
,
LINC01020
,
NDUFS6
,
LOC107986396
,
SNORD123
,
H3P18
,
LOC105374643
,
RPL9P17
,
LINC01511
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478004
variant
3.

nsv3887142

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H3Y1
,
CTD-2350J17.1
,
TMEM183AP2
,
LINC02221
,
FBXL7
,
CDH6
,
LINC01018
,
LOC107986401
,
LOC645763
,
ADCY2
,
LINC02145
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48450497
variant
4.

nsv3910712

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ROPN1L
,
RN7SKP73
,
LINC01020
,
RNU6-363P
,
SDHAP3
,
LINC01511
,
LOC105374706
,
LOC107986376
,
LINC02982
,
H3P19
,
DYNC1LI1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474067
variant
5.

nsv3924496

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374678
,
MIR4278
,
LOC107986405
,
LOC100419318
,
MIR4458HG
,
LINC02100
,
LINC02218
,
LINC02103
,
LOC105374672
,
LOC101929645
,
LOC105374655
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487851
variant
6.

nsv6636942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374608
,
LSP1P3
,
MIR4458
,
LOC105374651
,
LOC107986401
,
LINC01017
,
LINC02221
,
LINC02064
,
NUP50P3
,
CTD-2350J17.1
,
FBXL7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355771
variant
7.

nsv6636606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BASP1
,
RNU1-76P
,
ADAMTS16-DT
,
HSPD1P1
,
MARK2P5
,
LINC01194
,
CLPTM1L
,
H3P21
,
LOC105374618
,
HNRNPKP5
,
TPPP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355435
variant
8.

nsv3881706

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IRX2-DT
,
CEP72-DT
,
LINC02218
,
TENT4A
,
LOC107986405
,
CDH10
,
LOC105374695
,
BRD9
,
LOC100420683
,
SDHAP3
,
LOC101929307
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445061
variant
9.

nsv3883796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H3P22
,
PDCD6-AHRR
,
IRX2
,
LINC02142
,
SPCS2P3
,
LOC101929617
,
IRX4-AS1
,
LOC100421308
,
MIR4457
,
ICE1
,
RBBP4P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447151
variant
10.

nsv6315416

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374649
,
LINC02196
,
LOC101929645
,
LOC100422687
,
TENT4A
,
LOC105374669
,
PPP1R2P8
,
MARCHF11-DT
,
LOC107984098
,
MTRR
,
LOC105374672
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680363
variant
11.

nsv3912696

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OTULINL
,
LINC02111
,
CTD-2154B17.1
,
LOC105374630
,
AKTIPP2
,
RNA5SP179
,
MTND6P2
,
MIR4456
,
LINC02063
,
LOC107986377
,
PDCD6P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476051
variant
12.

nsv5381771

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OTULINL
,
AKTIPP2
,
LOC107986377
,
RN7SKP133
,
LINC02063
,
LINC02149
,
CEP72
,
LOC102723561
,
LOC100506858
,
LOC105374630
,
RBBP4P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51637028
variant
13.

nsv3916877

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CTD-2154B17.1
,
MIR10397
,
AHRR
,
MRPL36
,
IRX4-AS1
,
MIR4456
,
PDCD6-AHRR
,
OTULINL
,
MIR4457
,
SPCS2P3
,
PDCD6P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480232
variant
14.

nsv3922865

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCT6P2
,
LOC105374661
,
NACAP6
,
LSINCT5
,
LOC105374618
,
LOC101929359
,
LINC02100
,
LOC105374678
,
LINC02150
,
LOC107986345
,
RPL36AP21
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486220
variant
15.

nsv3916127

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929898
,
ZDHHC11
,
SLC6A3
,
TRPC6P6
,
TAF11L3
,
TRIP13
,
LINC02149
,
ZNF622
,
EXOC3-AS1
,
LOC107986403
,
LOC100132773
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479482
variant
16.

nsv3914997

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02241
,
SPICP4
,
RN7SL58P
,
TERT
,
LOC105374636
,
LOC100132773
,
LINC02239
,
SLC6A18
,
LOC105374656
,
RNU6-679P
,
PMCHL1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478352
variant
17.

nsv3917481

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC645763
,
LINC02221
,
LINC01017
,
CTD-2350J17.1
,
RNA5SP177
,
MTCO1P31
,
LOC107986401
,
LOC100130063
,
LINC02121
,
MIR4458
,
ALG3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480836
variant
18.

nsv3923396

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02899
,
TERLR1
,
MARCHF11
,
MIR4637
,
LPCAT1
,
SDHA
,
MARCHF6
,
GUSBP1
,
LOC100270647
,
NUP50P3
,
MTCYBP37
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486751
variant
19.

nsv3887688

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02223
,
BTG4P1
,
LINC02116
,
TERT
,
ANKH
,
IRX1
,
CDH9
,
LOC105374625
,
RETREG1
,
MSNP1
,
LOC105374682
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48451043
variant
20.

nsv4349271

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4636
,
LRRC14B
,
LOC100310782
,
EXOC3
,
CTD-2194D22.4
,
MARCHF6-DT
,
MIR6131
,
LOC107983966
,
OTULIN
,
MTRR
,
LOC102724943
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344184
variant
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