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Items: 20

1.

nsv3884707

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDST4
Location information:
Clinical significance:
Benign
ID:
48448062
variant
2.

nsv3881239

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRPS33P3
,
NDST4
Location information:
Clinical significance:
Benign
ID:
48444594
variant
3.

nsv3921840

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDST4
,
MRPS33P3
Location information:
Clinical significance:
Likely benign
ID:
48485195
variant
4.

nsv4728940

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDST4
,
MRPS33P3
Location information:
Clinical significance:
Likely benign
ID:
50372577
variant
5.

nsv4729325

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRPS33P3
,
NDST4
Location information:
Clinical significance:
Likely benign
ID:
50372962
variant
6.

nsv6290265

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105379404
,
IL21-AS1
,
TUBAP10
,
RPL7AP28
,
LARP1B
,
ACTN4P1
,
LOC105377409
,
TRC-GCA2-1
,
TECRP2
,
LOC105377406
,
SETP12
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53634142
variant
7.

nsv3873978

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100422029
,
H2AZ1
,
LOC101928217
,
LINC02435
,
RHOH
,
RNU6-35P
,
DCK
,
CEP44
,
LOC105378242
,
RN7SL492P
,
LOC105374392
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437333
variant
8.

nsv3876533

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100420289
,
LOC100131038
,
HS3ST1
,
UGDH
,
MTATP6P9
,
LOC105377495
,
RNU6-310P
,
TBCK
,
AGA-DT
,
MYL5
,
LOC105377604
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439888
variant
9.

nsv3884499

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND4LP29
,
RNU6-128P
,
LINC01258
,
LOC101927179
,
LINC02173
,
CTBP1-AS
,
GALNT7-DT
,
LOC391711
,
TBC1D1
,
SUMO2P11
,
RN7SKP235
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447854
variant
10.

nsv3880085

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268460
,
LINC02435
,
MIR576
,
RN7SL492P
,
PRMT5P1
,
DEFB108F
,
LOC100422029
,
USP17L24
,
LINC00575
,
TAPT1
,
LINC02503
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443440
variant
11.

nsv3883791

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377343
,
PDGFC
,
LOC105374535
,
RPL7AP29
,
LOC101928893
,
GATB
,
LOC102723704
,
LOC101928658
,
LOC105377558
,
NAAA
,
LOC107986328
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447146
variant
12.

nsv3875534

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KLKB1
,
NDST3
,
LOC112268472
,
NDST4
,
MTND3P3
,
ZGRF1
,
LSM6
,
PRSS48
,
LOC100287014
,
RNU6-1217P
,
TENM3-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438889
variant
13.

nsv6291432

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNHG27
,
TNIP3
,
KPNA2P1
,
RNU6-699P
,
RNU6-224P
,
LYPLA1P2
,
TMPRSS11A
,
HMGB3P15
,
RNU6-1252P
,
UBE2CP3
,
LINC02485
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53636827
variant
14.

nsv3874596

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL6P12
,
F11
,
GK3
,
TENM3-AS2
,
LRBA
,
ING2-DT
,
GPM6A-DT
,
LOC107986192
,
KLKB1
,
LOC100287014
,
TLL1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437951
variant
15.

nsv6313878

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC00613
,
GYPA
,
LOC101927636
,
PIMREGP2
,
LOC105377375
,
LOC105377378
,
RNU6-1054P
,
ETNPPL
,
LOC107986237
,
ARHGEF38-IT1
,
LARP7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677749
variant
16.

nsv3920388

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR576
,
ABT1P1
,
LOC102723967
,
AIMP1
,
LINC02435
,
TIFA
,
CYP2U1
,
COILP2
,
CAMK2D
,
NDUFS5P4
,
LOC107986231
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483743
variant
18.

nsv3885667

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR577
,
RN7SL808P
,
CIR1P2
,
UGT8
,
NDST4
,
LOC105377382
Location information:
Clinical significance:
Uncertain significance
ID:
48449022
variant
19.

nsv3916316

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-194P
,
FOSL1P1
,
RN7SL253P
,
LOC441052
,
METTL14-DT
,
UFSP2
,
LOC105377376
,
SFRP2
,
RNU6-205P
,
LINC02514
,
LOC100287014
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48479671
variant
20.

nsv3872274

ID:
48435629
variant
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