"estd208"[study] AND "deletion"[variant_type] - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 20 of 35

<< First< Prev

Page of 2

1.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: DMD

Location information:

ID:: 16965019

variant

2.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: DMD

Location information:

ID:: 16965070

variant

3.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: NRXN1; NRXN1-DT

Location information:

ID:: 16965038

variant

4.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: ADGRL4; PSAT1P3

Location information:

ID:: 16965004

variant

5.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: PDE1A; LOC101929976

Location information:

ID:: 16965003

variant

6.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: LOC105374004; LOC107986104

Location information:

ID:: 16965037

variant

7.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: MAB21L1; NBEA

Location information:

ID:: 16965066

variant

8.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: PDE4D; RAB3C; RPL5P15

Location information:

ID:: 16965028

variant

9.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: LOC105377378; LOC105377379; LOC107986235

Location information:

ID:: 16965029

variant

10.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: STX8; CFAP52; RPL19P18

Location information:

ID:: 16965056

variant

11.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: FABP4; PMP2; FABP9; LOC101927118

Location information:

ID:: 16965043

variant

12.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: CDH13; LOC101928446; RN7SL134P

Location information:

ID:: 16965010

variant

13.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: ADPRM; TMEM220; TMEM238L; MAGOH2P; TMEM220-AS1

Location information:

ID:: 16965001

variant

14.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: COMMD10; RPS25P6; ARL14EPL

Location information:

ID:: 16965044

variant

15.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: ADGRB1; ARC; MROH4P

Location information:

ID:: 16965049

variant

16.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: CNTN4; RPL23AP38; RPL21P17; RPL23AP39; CNTN4-AS2; HINT2P1; RN7SKP144

Location information:

ID:: 16965026

variant

17.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: SHOX; GTPBP6; PPP2R3B; PLCXD1; LINC00685; LOC102724521; KRT18P53; FABP5P13

Location information:

ID:: 16965013

variant

18.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: ACAT2; CCR6; GNG5P1; GPR31; IGF2R; KIF25; LPA; MAS1; MAP3K4; AFDN; PRKN; PDCD2; PLG; PSMB1; RPS6KA2; SLC22A1; SLC22A3; SLC22A2; SOD2; TBXT; TBP; TCP1; TCP10L3; DYNLT2; DYNLT1; THBS2; EZR; RNASET2; SYNJ2; QKI; WTAP; PDE10A; CEP43; LINC01558; DLL1; MRPL18; SNX9; MPC1; UNC93A; PHF10; ERMARD; AGPAT4; TULP4; TMEM181; SMOC2; FRMD1; AGPAT4-IT1; LINC00574; LPAL2; OR4F7P; RSPH3; TTLL2; FAM120B; FNDC1; SERAC1; LINC00473; SYTL3; SFT2D1; TAGAP; PACRG; SRP72P2; PNLDC1; LOC154449; DACT2; C6orf118; OSTCP1; WDR27; PACRG-AS1; PRR18; LOC285804; GAPDHP72; RAMACL; C6orf120; DKFZp451B082; TCP10L2; LINC02538; LINC00242; LINC01624; GTF2H5; LINC00602; LINC02487; LOC441179; LOC442272; RPL21P69; LOC645468; AFDN-DT; SNORA20; SNORA29; CHP1P2; PACRG-AS3; LOC729681; HGC6.3; SOD2-OT1; KRT8P44; LINC02901; LOC100131532; HNRNPH1P1; TRE-TTC15-1; RPL12P23; RPL34P15; RPL37AP4; AIRN; TATDN2P2; LOC100289495; MIR1913; LOC100420305; AMZ2P2; LOC100421518; CTAGE13P; LOC100422263; MIR3918; MIR3939; KIF25-AS1; CAHM; MIR4644; RPS6KA2-AS1; SYNJ2-IT1; RPS6KA2-IT1; EZR-AS1; FNDC1-AS1; LOC101929142; PACRG-AS2; LOC101929297; LOC101929420; LOC101929460; LINC01615; LINC02544; THBS2-AS1; LOC101929614; MIR7161; LINC02529; LOC102724087; LOC102724152; LOC102724220; LOC102724357; LOC102724511; LOC102725048; LOC105369171; SNX9-AS1; TAGAP-AS1; LOC105378084; LOC105378085; LOC105378088; LOC105378093; LOC105378094; LOC105378095; LOC105378097; LOC105378098; LOC105378099; LOC105378100; LOC105378102; LOC105378104; LOC105378106; LOC105378109; MEAT6; LOC105378113; LOC105378114; LOC105378115; LOC105378116; LOC105378117; LOC105378118; LOC105378119; LOC105378120; LOC105378123; LOC105378126; LOC105378127; LOC105378128; LOC105378129; LOC105378130; LOC105378131; LOC105378135; LOC105378137; LOC105378139; LOC105378140; LOC105378141; LOC105378142; LOC105378143; LOC105378144; LOC105378145; LOC105378146; LINC02519; LOC105378148; LOC105378149; LOC105378150; LOC105378153; LOC105378157; LOC105379712; RNA5SP226; RN7SL173P; RNU6-153P; RNU6-730P; WBP1LP8; CACYBPP3; RN7SL366P; RNU6-293P; RNU6-786P; HNRNPA1P49; HSPE1P26; VTA1P1; RNU4ATAC18P; LOC107986546; LOC107986547; LOC107986548; LOC107986549; LOC107986550; LOC107986665; LOC107986667; LOC107986668; LOC107986669; LOC107986671; LOC107986672; LOC107986673; LOC107986674; LOC107986675; LOC107986676; SNORA116; LOC112267968; LOC112267969; LOC112267970; LOC112267977; HPAT5; See more...

Location information:

ID:: 16965054

variant

19.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: ATP2B2; CAV3; FANCD2; GRM7; IL5RA; IRAK2; ITPR1; OGG1; OXTR; SEC13; SETMAR; VHL; BRPF1; CAMK1; BHLHE40; EDEM1; TATDN2; SRGAP3; ARPC4; TADA3; CHL1; THUMPD3; TTLL3; CNTN6; LINC00312; LMCD1; SSUH2; TRNT1; CRBN; GHRL; ARL8B; SETD5; EMC3; BRK1; RAD18; LRRN1; CIDEC; MTMR14; CRELD1; OR7E122P; JAGN1; LINC00852; IL17RC; FANCD2OS; IL17RE; CPNE9; CIDECP1; CNTN4; SUMF1; RPUSD3; PRRT3; MRPS35P1; MRPS36P1; MRPS10P2; CYCSP10; CYCSP11; LHFPL4; RPL23AP38; PGAM1P4; RPSAP32; THUMPD3-AS1; EMC3-AS1; UBTFL8; DUSP5P2; RPL21P17; MIR885; EGOT; GHRLOS; LOC100130207; RPS8P6; RPL23AP39; LMCD1-AS1; PNPT1P1; SRGAP3-AS3; RNF10P1; FANCD2P1; MARK2P1; MARK2P2; MIR378B; BHLHE40-AS1; ARPC4-TTLL3; MIR4790; GRM7-AS1; CNTN4-AS1; CNTN4-AS2; PRRT3-AS1; ATP2B2-IT2; ITPR1-DT; CHL1-AS2; CHL1-AS1; LINC01266; GRM7-AS3; LOC101927394; SRGAP3-AS2; SRGAP3-AS4; HINT2P1; LINC01986; LOC102723512; LOC102723596; LOC105376921; LOC105376922; LOC105376923; LOC105376924; LOC105376926; LOC105376933; LOC105376936; LOC105376938; LOC105376939; LOC105376940; LOC105376941; LOC105376942; LOC105376943; LOC105376944; LOC105376945; GRM7-AS2; LOC105376949; RN7SKP144; RNU6-670P; CRB3P1; RN7SL553P; DNAJC19P4; RNU4ATAC17P; RN7SL120P; RNU6-882P; RNU6-1194P; LOC107984112; LOC107986009; LOC107986010; LOC107986040; LOC107986057; LOC107986058; LOC107986059; LOC107986061; MIR12127; See more...

Location information:

ID:: 16965072

variant

20.

Variant type:: copy number variation

Associated study:: estd208

Organism:
human

Genes(s) in region:: ACVR1; ATP5F1AP2; GPD2; KCNJ3; NR4A2; PKP4; CYTIP; GALNT5; ERMN; ACVR1C; CCDC148; UPP2; CDK7P1; FLJ46875; CCDC148-AS1; CBX3P6; FAM133DP; HNRNPDLP2; HEBP2P1; MTA3P1; TRA-CGC3-1; TRG-GCC2-2; RPLP0P7; PTP4A1P1; MTND2P20; MTND4P28; MTND5P30; LINC01876; LOC105373696; LOC105373698; LOC105373699; LOC105373700; LOC105373703; LOC105373707; LINC01958; LOC105373709; LOC105373710; LOC105373712; LOC105373714; MTND6P9; RNU6-546P; RN7SKP281; RNU6-1001P; RNU6-436P; RNU6-932P; RN7SL393P; MTCYBP9; MTCO1P45; LOC107985828; LOC107985952; LOC107985953; See more...

Location information:

ID:: 16965007

variant

<< First< Prev

Page of 2

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

"estd208"[study] AND "deletion"[variant_type] (36)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)