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Items: 17

1.

nsv7095484

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NCSTN
,
COPA
Location information:
Clinical significance:
Uncertain significance
ID:
55275673
variant
2.

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
3.

nsv3889882

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FMO4
,
RPL30P1
,
FMO1
,
FMO6P
,
LMX1A
,
RN7SL861P
,
NCSTN
,
ATP1A2
,
RPL7AP21
,
TRD-GTC2-2
,
ADCY10
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453237
variant
4.

nsv4450412

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FCGR3B
,
SLAMF9
,
RPS13P1
,
CFAP45
,
TRG-TCC2-3
,
IGSF9
,
RGS4
,
LOC105371459
,
LOC107985213
,
FCGR2A
,
ATF6-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49616047
variant
5.

nsv3906717

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NOS1AP
,
LY9
,
TRD-GTC2-5
,
TRE-CTC1-5
,
VANGL2
,
LOC100420658
,
B4GALT3
,
FCGR3A
,
ITLN2
,
PCP4L1
,
CD84
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470072
variant
6.

nsv3884593

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR10AE1P
,
USP21
,
LOC105371466
,
ATF6
,
RNU6-481P
,
RPS23P9
,
SLAMF1
,
TRL-CAG1-1
,
VSIG8
,
LOC102724602
,
FCGR2B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447948
variant
7.

nsv3877365

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MARK1
,
LINC02766
,
FDPS
,
PRUNE1
,
GJB4
,
RN7SL653P
,
PPIEL
,
CRB1
,
SELENBP1
,
LBR
,
CHML
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440720
variant
8.

nsv3885206

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP47
,
STK40
,
RNU6-750P
,
LINC01138
,
MIR4632
,
LOC107985100
,
EIF2D
,
SEPTIN7P13
,
RAB13
,
LOC107985524
,
DR1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448561
variant
9.

nsv3884414

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU1-153P
,
MIR3917
,
LOC105378793
,
CCDC190
,
RPL29P6
,
RUNX3-AS1
,
MIXL1
,
LCE1B
,
NAXE
,
PDC-AS1
,
BNIPL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447769
variant
10.

nsv3918947

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101060227
,
LINC01720
,
LOC105371693
,
LINC01350
,
DCST1
,
PTPN2P1
,
SCYL3
,
GYG2P2
,
KIAA1614-AS1
,
KISS1
,
LOC105371610
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482302
variant
11.

nsv3900459

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HORMAD1
,
BCAN-AS1
,
OR10K2
,
TSTD1
,
VHLL
,
S100A5
,
MIR1295B
,
RPS11P3
,
GOLPH3L
,
GPR52
,
RNU5F-6P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463814
variant
12.

nsv3890224

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101928596
,
KCNJ10
,
LOC100506023
,
OR6P1
,
LOC107985224
,
FCRL1
,
DUSP12
,
RPS23P10
,
HSPA7
,
LINC01363
,
LOC107985453
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453579
variant
13.

nsv5381285

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DCST1
,
NUDT17
,
THEM5
,
RPS15AP12
,
LOC100271842
,
LOC100216488
,
LOC107985464
,
LOC105371438
,
GORAB
,
B4GALT3
,
SRGAP2D
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
51636542
variant
14.

nsv6310595

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGSF8
,
SETP9
,
FCER1A
,
TRG-GCC2-1
,
HSPA6
,
OLFML2B
,
RRM2P2
,
AIM2
,
TRE-CTC1-2
,
SLAMF6P1
,
TRD-GTC2-4
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53674466
variant
15.

nsv4450321

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985216
,
PPIAP37
,
LOC646347
,
F11R
,
SLAMF9
,
CASQ1
,
CFAP45
,
CD244
,
IGSF9
,
LOC105371466
,
SLAMF1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49615956
variant
16.

nsv6637035

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PEX19
,
SLAMF8
,
KCNJ10
,
ATP1A4
,
ATP1A2
,
RNU4-42P
,
LOC729867
,
CFAP45
,
SLAMF9
,
CASQ1
,
LOC107985216
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54355864
variant
17.

nsv6310733

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SUMO1P3
,
NCSTN
,
ATP1A4
,
ATP1A2
,
PEX19
,
LOC729867
,
CASQ1
,
COPA
,
DCAF8
,
RPSAP18
,
PEA15
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53674604
variant
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