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Items: 15

1.

nsv7095201

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TYROBP
Location information:
Clinical significance:
Pathogenic
ID:
55275390
variant
2.

nsv5672902

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TYROBP
Location information:
Clinical significance:
not provided
ID:
52234037
variant
3.

nsv3919296

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UBA2
,
ZNF529
,
SCGB1B1P
,
LRP3
,
LOC100128948
,
RPS4XP21
,
APLP1
,
LOC105372371
,
LINC01791
,
LRFN3
,
ZNF571-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482651
variant
4.

nsv3916007

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MAG
,
RNU6-967P
,
ZBTB32
,
LOC107985271
,
HPN
,
SCGB2B1P
,
ZNF566-AS1
,
PEPD
,
RN7SKP22
,
LINC01766
,
LOC100134317
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479362
variant
6.

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
7.

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
8.

nsv3903092

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LENG8
,
SYDE1
,
FBN3
,
ZNF419
,
ZNF793
,
RNU4-60P
,
LOC105372420
,
NAPSA
,
CARM1
,
KEAP1
,
ZNF14
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466447
variant
9.

nsv3913730

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BCKDHA
,
ADGRE5
,
CLEC17A
,
VN1R83P
,
SNORA68B
,
LOC105372370
,
MAN2B1
,
PGK1P2
,
AKAP8L
,
ZNF567-DT
,
CC2D1A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477085
variant
10.

nsv6290300

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF420
,
LOC105372330
,
BNIP3P31
,
LOC105372353
,
RPL36AP51
,
RN7SL491P
,
SCGB2B2
,
ZNF676
,
SNX6P1
,
ZNF565
,
IFNL2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53634177
variant
11.

nsv4457372

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF461
,
LOC101927572
,
TPM3P5
,
CEACAM22P
,
LOC105372405
,
MAP4K1
,
CEACAMP6
,
SELENOW
,
CADM4
,
ETV2
,
BSPH1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49623007
variant
13.

nsv3902356

ID:
48465711
variant
15.

nsv6291710

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NFKBID
,
APLP1
,
LRFN3
,
GAPDHS
,
U2AF1L4
,
LINC01529
,
IGFLR1
,
HAUS5
,
CLIP3
,
PROSER3
,
RN7SL402P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53637105
variant
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