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Items: 1 to 20 of 44

1.

nsv3884752

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPD1
,
HSPE1-MOB4
,
HSPE1
,
SNORA105B
Location information:
Clinical significance:
Uncertain significance
ID:
48448107
variant
2.

nsv5381571

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPE1
,
SNORA105B
,
HSPE1-MOB4
,
HSPD1
Location information:
Clinical significance:
Uncertain significance
ID:
51636828
variant
3.

nsv3910630

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DAZAP2P1
,
RPL36AP16
,
TRIM51JP
,
LOC105373608
,
LOC105373903
,
LOC105374690
,
C2orf81
,
LOC105377627
,
LOC105373714
,
C2orf78
,
ELF2P4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473985
variant
4.

nsv3894939

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRE-TTC9-1
,
DNAJC19P5
,
LINC01923
,
RBM45
,
TMEFF2
,
NABP1
,
PJVK
,
LOC107985968
,
LOC107985965
,
CASP10
,
KCTD18
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458294
variant
5.

nsv6315398

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985785
,
MYO1B
,
SF3B1
,
DSTNP5
,
GAPDHP59
,
ZDBF2
,
OSGEPL1-AS1
,
PLEKHM3
,
STK17B
,
NIF3L1
,
LOC105373823
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680345
variant
6.

nsv3899404

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01877
,
MFSD6
,
LOC105373770
,
DIRC1
,
C2orf66
,
LOC105373793
,
CAVIN2-AS1
,
LOC105373796
,
LOC105373833
,
LOC105373836
,
LOC105373816
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48462759
variant
7.

nsv3896612

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND4P30
,
NPM1P46
,
VWC2L-IT1
,
SNORD70
,
NPM1P33
,
MIR4776-2
,
C2orf69
,
NOP58
,
LOC100533727
,
RNU1-133P
,
CFLAR
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459967
variant
8.

nsv3895293

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CALCRL-AS1
,
ZC3H15
,
LOC105373766
,
COL5A2
,
HECW2-AS1
,
OSGEPL1-AS1
,
RPL23AP33
,
LOC107985831
,
RPL4P7
,
E2F3P2
,
LOC105373780
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458648
variant
9.

nsv6637127

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100421409
,
LOC100507443
,
MTCO3P17
,
ASDURF
,
MTCO2P17
,
UBE2V1P11
,
LOC105373855
,
SNORD11B
,
LOC105373812
,
RNU6-169P
,
LINC01802
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355956
variant
10.

nsv3891560

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AOX1
,
RPL23AP35
,
IMPDH1P7
,
STAT4-AS1
,
HMGB1P27
,
RN7SL820P
,
NAB1
,
LOC105373788
,
LOC100420572
,
ANKRD44-IT1
,
LOC105373828
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454915
variant
11.

nsv6636571

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GAPDHP59
,
OSGEPL1-AS1
,
MYO1B
,
LOC105373823
,
LOC107985785
,
SF3B1
,
MIR1245A
,
ZC3H15
,
STK17B
,
RNU6-989P
,
ANKRD44
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355400
variant
13.

nsv3884912

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLK1
,
RNU6-762P
,
RNY4P34
,
LOC729254
,
CASP10
,
TMEFF2
,
NIF3L1
,
LINC01923
,
KCTD18
,
COQ10B
,
NABP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448267
variant
16.

nsv3908231

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01877
,
MAIP1
,
PIMREGP1
,
KRT8P52
,
BOLL
,
SNORD70B
,
BICD1P1
,
RPL7P14
,
LOC105373836
,
AOX3P-AOX2P
,
RNU6-1029P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471586
variant
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