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Items: 13

1.

nsv7095207

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LTBP4
Location information:
Clinical significance:
Uncertain significance
ID:
55275396
variant
2.

nsv6310634

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LTBP4
Location information:
Clinical significance:
Uncertain significance
ID:
53674505
variant
3.

nsv7095208

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LTBP4
,
NUMBL
,
COQ8B
Location information:
Clinical significance:
Uncertain significance
ID:
55275397
variant
4.

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
5.

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
6.

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
7.

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
8.

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
9.

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
10.

nsv3912447

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR8077
,
TRI-TAT1-1
,
GRIK5
,
MTND5P45
,
ARHGEF1
,
CXCL17
,
RPS29P26
,
DNAJC19P2
,
ZFP36
,
CEACAM4
,
CEACAMP3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475802
variant
11.

nsv3895066

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-140P
,
COQ8B
,
RPS29P24
,
FCGBP
,
SPRED3
,
MIR641
,
ZNF527
,
LOC100129935
,
ZNF546
,
ZNF420
,
DLL3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458421
variant
13.

nsv7095278

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HIPK4
,
PRX
,
SERTAD3-AS1
,
SHKBP1
,
SPTBN4
,
PLD3
,
LTBP4
,
BLVRB
,
SERTAD3
,
SERTAD1
Location information:
Clinical significance:
Uncertain significance
ID:
55275467
variant
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