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Items: 12

1.

nsv3904885

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF321P
,
ZNF861P
,
ZNF816
,
ARID3A
,
MIR642B
,
LOC105372295
,
LOC105372424
,
PTOV1-AS2
,
SLC8A2
,
LOC105372401
,
ZNF419
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468240
variant
2.

nsv3903203

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BABAM1
,
BEST2
,
CALR3
,
SNAR-A8
,
RFPL4AP1
,
RPL39P35
,
OSTCP3
,
LOC105372291
,
SLC25A36P1
,
ZNF653
,
SCN1B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466558
variant
3.

nsv3919076

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNA7
,
ZNF28
,
LOC105372435
,
RNU6-980P
,
ZNF837
,
SNAR-A11
,
SNAR-A6
,
RPL36AP50
,
RPL7AP69
,
LOC105372441
,
SIGLEC26P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482431
variant
4.

nsv3924732

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL39P37
,
CCDC106
,
SHISA7
,
ERVV-2
,
KLK7
,
LOC107985347
,
TNNT1
,
ZNF17
,
ZNF816
,
SIGLEC17P
,
ZNF470
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48488087
variant
5.

nsv3890862

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SIGLECL1
,
KLK5
,
SIGLEC9
,
KLK9
,
ZSCAN5C
,
LOC101928804
,
ZNF534
,
NDUFV2P1
,
NAPSA
,
KLK2
,
MIR512-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454217
variant
6.

nsv3923909

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OSCAR
,
FKBP1AP1
,
ZNF671
,
OSTCP3
,
LOC105372442
,
IZUMO2
,
LOC105372439
,
LINC02560
,
LOC284379
,
SIGLEC27P
,
MIR935
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487264
variant
7.

nsv3891963

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS9
,
ZNF480
,
VN1R6P
,
LOC102724273
,
MIR517B
,
RN7SKP109
,
LINC01869
,
ZNF749
,
LOC100419707
,
VN1R103P
,
ZNF702P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455318
variant
8.

nsv3923613

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF71-SMIM17
,
MIR518E
,
LOC100419839
,
DNAAF3-AS1
,
RPLP1P12
,
MIR520G
,
ZNF773
,
LAIR1
,
RPL28
,
MYADM
,
ZNF611
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486968
variant
9.

nsv3919766

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR520F
,
A1BG-AS1
,
MIR10394
,
KIR3DX1
,
ZNF581
,
LILRA5
,
MIR1323
,
TMEM150B
,
MIR517C
,
MIR522
,
LOC107985346
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483121
variant
11.

nsv3910645

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF132
,
ZNF324
,
ZNF446
,
RN7SL525P
,
ZNF324B
,
RN7SL693P
,
CENPBD2P
,
ZNF584
,
MIR6807
,
UBE2M
,
RNU6-1337P
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
48474000
variant
12.

nsv3922528

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UBE2M
,
TRIM28
,
CHMP2A
,
CENPBD2P
,
MZF1
,
MZF1-AS1
,
MIR6807
Location information:
Clinical significance:
Benign
ID:
48485883
variant
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