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Items: 1 to 20 of 28

1.

nsv3900719

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CREB5
Location information:
Clinical significance:
Benign
ID:
48464074
variant
2.

nsv3897632

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CREB5
Location information:
Clinical significance:
Benign
ID:
48460987
variant
3.

nsv3919826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-438P
,
LOC105375300
,
URGCP
,
MOXD2P
,
LOC105375171
,
SP4
,
LOC105375194
,
LOC105375277
,
TRBV21-1
,
MIR4283-1
,
VN1R24P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483181
variant
4.

nsv3888815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986817
,
DNAJB9
,
LRRN3
,
SKAP2
,
LOC107986794
,
MAGI2-AS2
,
CPA2
,
MIR10525
,
VN1R37P
,
SPDYE7P
,
DPY19L1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452170
variant
5.

nsv3922885

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IL6-AS1
,
HOXA10-AS
,
LINC02860
,
SNX2P2
,
RPL7AP41
,
TAX1BP1
,
LOC105375206
,
PSMC1P2
,
NUP42
,
PLEKHA8
,
LINC03095
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486240
variant
6.

nsv3892894

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NPVF
,
RNU6-1103P
,
HOXA4
,
RNA5SP228
,
RPS2P30
,
CLK2P1
,
TAX1BP1-AS1
,
SNORD65C
,
GPNMB
,
HOXA1
,
JAZF1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456249
variant
7.

nsv4674822

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RP9P
,
LINC00997
,
NFE2L3
,
MIR550A3
,
MIR148A
,
LOC107986699
,
LOC107986782
,
LOC646762
,
ADCYAP1R1
,
CHN2-AS1
,
MTURN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271647
variant
8.

nsv6315453

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLEKHA8
,
NFE2L3
,
RPS29P14
,
LINC00997
,
MIR148A
,
RP9P
,
FKBP14
,
LOC105375206
,
LOC646762
,
LOC107986733
,
HOXA5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680400
variant
9.

nsv4435897

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC126
,
LOC389473
,
LOC105375200
,
PRR15
,
MALSU1
,
RPL7AP38
,
GGCT
,
TPM3P4
,
LOC442517
,
SUMO2P14
,
HOXA10-AS
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49579501
variant
12.

nsv3894780

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-565P
,
LAMB1
,
MIR5707
,
LOC100419774
,
ZNF786
,
ELK1P1
,
MTCYBP42
,
SSU72L6
,
EEF1A1P27
,
LOC105375200
,
THUMPD3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458135
variant
13.

nsv4455091

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP51
,
FLJ40288
,
STAG3L2
,
FKBP9
,
BNIP3P11
,
GPR37
,
LOC105375251
,
LOC100419642
,
LOC105375148
,
PMS2P7
,
TRBV10-3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49620726
variant
14.

nsv3909087

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MNX1-AS2
,
VN1R31P
,
PRSS58
,
LOC107986715
,
AHCYL2
,
BAIAP2L1
,
LOC107986821
,
NUPR2
,
SEPTIN7P4
,
PRKAR1B
,
TRBV15
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472442
variant
15.

nsv3908592

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRGV3
,
SNX10-AS1
,
LOC105375433
,
LOC101060796
,
OR9A2
,
LOC105375542
,
SPDYE2
,
NPY
,
RNU6-979P
,
RN7SL265P
,
RNY4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471947
variant
16.

nsv3915802

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP52
,
IQCE
,
LOC101928421
,
TRGJP2
,
CARD11
,
NUP42
,
FBXL18
,
TAX1BP1
,
RBAK-RBAKDN
,
LOC100533631
,
RPL26P21
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479157
variant
17.

nsv3899194

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BRWD1P3
,
TRGV10
,
LOC105375206
,
LOC100133177
,
TRG-AS1
,
GTF3C6P3
,
LOC105375183
,
LOC107986787
,
CDC14BL
,
LOC401324
,
GTF2IP13
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48462549
variant
18.

nsv3918785

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MMD2
,
ICA1-AS1
,
VWDE
,
EIF3B
,
TNRC18
,
SDK1
,
RPS26P30
,
LOC105375187
,
LOC105375207
,
ZFAND2A
,
PRR15-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482140
variant
19.

nsv3903410

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100131264
,
SP4
,
FCF1P1
,
RPL6P21
,
LOC105375211
,
IMMP1LP3
,
DGKB
,
LOC112267993
,
HOXA-AS3
,
RPSAP73
,
LOC105375131
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466765
variant
20.

nsv3895449

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HOXA7
,
SNX13
,
PPP1R14BP4
,
HOTTIP
,
HOXA10-HOXA9
,
HOXA11
,
INMT
,
SP4
,
LOC105375208
,
LOC105375211
,
DGKB
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458804
variant
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