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Items: 1 to 20 of 63

1.

nsv4455544

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NSMCE2
Location information:
Clinical significance:
Pathogenic
ID:
49621179
variant
2.

nsv7097785

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NSMCE2
Location information:
Clinical significance:
Pathogenic
ID:
55277974
variant
3.

nsv4675167

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NSMCE2
Location information:
Clinical significance:
Likely benign
ID:
50271992
variant
4.

nsv3912704

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
WASHC5
,
NSMCE2
Location information:
Clinical significance:
Uncertain significance
ID:
48476059
variant
5.

nsv3923568

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
WASHC5
,
NSMCE2
Location information:
Clinical significance:
Uncertain significance
ID:
48486923
variant
6.

nsv6312901

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL329P
,
NSMCE2
Location information:
Clinical significance:
Uncertain significance
ID:
53676772
variant
7.

nsv3902676

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02964
,
WASHC5
,
TRIB1
,
RN7SL329P
,
NSMCE2
Location information:
Clinical significance:
Benign
ID:
48466031
variant
8.

nsv7097650

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NSMCE2
,
RN7SL329P
,
WASHC5
Location information:
Clinical significance:
Uncertain significance
ID:
55277839
variant
9.

nsv3903593

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NSMCE2
,
TRIB1
,
LINC02964
Location information:
Clinical significance:
Uncertain significance
ID:
48466948
variant
10.

nsv6637224

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-37P
,
LOC100420215
,
LOC102723447
,
SQLE-DT
,
SNORD168
,
LOC112268031
,
RNU6-12P
,
RNA5SP277
,
CCAT1
,
LOC105375721
,
LOC101927588
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54356053
variant
11.

nsv3876297

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZHX1-C8orf76
,
DEPTOR
,
LOC105375751
,
LOC100286746
,
MIR4663
,
LOC105375731
,
MIR6844
,
LOC107986903
,
LOC100133147
,
DERL1
,
LINC00964
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439652
variant
12.

nsv3914003

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-442P
,
ANXA13
,
RAD21
,
RNU6-875P
,
HAS2
,
MIR3610
,
LRATD2
,
RNF139-DT
,
LOC101927543
,
KNOP1P5
,
ATAD2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477358
variant
13.

nsv4455511

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTSS1
,
PCAT2
,
LINC02964
,
LOC105375769
,
EFR3A
,
ARF1P3
,
LOC105375743
,
PRNCR1
,
RN7SKP206
,
RN7SKP155
,
MIR4662B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621146
variant
16.

nsv3915173

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL474P
,
UNC5D
,
VN1R45P
,
MIOXP1
,
VIRMA
,
PRDM14
,
LOC100996662
,
ZFAT-AS1
,
C1GALT1P3
,
LOC105375779
,
LOC105375933
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478528
variant
17.

nsv3901821

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBC1D31
,
LOC105375740
,
ESCO2
,
MIR6847
,
TNFRSF10C
,
RHOBTB2
,
ATP6V1G1P2
,
LOC105375637
,
MTND5P41
,
RNU6-144P
,
MAFA
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465176
variant
18.

nsv4349554

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929488
,
TEX15
,
LOC105375789
,
MTND4LP26
,
LOC105379384
,
DEFA1B
,
MIR1302-7
,
PTP4A3
,
LOC101927997
,
LINC02990
,
XKR6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344467
variant
19.

nsv3916777

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL5P22
,
ARHGEF10
,
LOC107986952
,
FAM90A6P
,
LOC105375692
,
EFR3A
,
RNF139
,
NCAPGP1
,
LY6S
,
ZNNT1
,
CYCSP22
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480132
variant
20.

nsv3898123

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SPAG1
,
LOC101927657
,
PPIAP84
,
BMP1
,
TUSC3
,
LOC100129098
,
RPL10P18
,
LOC105375873
,
SQLE-DT
,
LOC105375638
,
SIRLNT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461478
variant
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