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See other FAM41C CNV Assays ›
Gene Symbol
FAM41C
Assay Reference Genome
Location

Chr.1:872506 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03336971_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 284593

Gene Name:

 family with sequence similarity 41 member C

Gene Aliases:

 -

Location:

 Chr.1:868071-876802 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM41C NR_027055.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv4n111 Chr.1:869076 - 914637 on Build GRCh38 Duplication FAM41C LOC284600
nsv1004962 Chr.1:629241 - 915295 on Build GRCh38 Gain LOC100288069 MTND2P28 LINC01128 MTND1P23 OR4F16 MIR6723 LOC107984841 LOC284600 FAM87B LOC100133331 LOC100287934 FAM41C LINC00115
nsv945739 Chr.1:865934 - 891159 on Build GRCh38 Duplication FAM41C
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss TMEM240 LOC100288069 MIR6808 AURKAIP1 C1orf159 SSU72 DDX11L1 PRKCZ MRPL20 ISG15 LOC101928626 TMEM52 MORN1 CALML6 FAAP20 CCNL2 SAMD11 MIR6726 ACAP3 FAM87B TAS1R3 LOC100506504 ATAD3B LOC100287934 LOC729737 LOC100130417 LOC107985728 LOC100132287 RNF223 LINC00115 FAM138A HES4 LOC148413 LOC105378592 MIR200A PERM1 OR4F16 LOC107984841 FNDC10 LOC100134822 DVL1 MIR6859-1 CPSF3L CDK11A OR4F29 TMEM88B SLC35E2B MIR6727 LOC102725121 SCNN1D TNFRSF18 LOC107985729 SDF4 WASH7P FAM132A MMP23A SKI MTND2P28 LINC01128 KLHL17 SLC35E2 VWA1 MIR200B TTLL10-AS1 LOC102724312 GABRD NADK TNFRSF4 NOC2L TTLL10 B3GALT6 MTND1P23 CPTP MIR429 MIR1302-2 ATAD3A CDK11B LOC105378947 ANKRD65 CFAP74 LOC105378948 UBE2J2 PUSL1 LINC01342 LOC100133331 LOC105378949 MMP23B GNB1 ATAD3C AGRN MIR6859-2 LOC105378591 MIR6723 OR4F5 LOC284600 PLEKHN1 LOC105378589 LOC100129534 FAM41C MIB2 MXRA8 LOC100288175
dgv1n67 Chr.1:811028 - 914557 on Build GRCh38 Gain FAM87B LINC01128 FAM41C LINC00115 LOC284600
nsv508924 Chr.1:854379 - 884949 on Build GRCh38 Insertion LINC01128 FAM41C
nsv1005935 Chr.1:805477 - 915295 on Build GRCh38 Gain FAM87B LINC01128 FAM41C LINC00115 LOC284600
nsv442837 Chr.1:830721 - 874393 on Build GRCh38 Gain+Loss LINC01128 FAM41C
esv3584981 Chr.1:837710 - 917284 on Build GRCh38 Loss LINC01128 FAM41C LOC100130417 LOC284600
nsv1009537 Chr.1:841742 - 915295 on Build GRCh38 Gain LINC01128 FAM41C LOC284600
dgv5n100 Chr.1:585989 - 1114424 on Build GRCh38 Gain LOC100288069 MTND2P28 PERM1 LINC01128 C1orf159 LOC105378948 KLHL17 OR4F16 LOC107984841 LOC100133331 NOC2L ISG15 LOC101928626 MTND1P23 AGRN SAMD11 MIR6723 LOC284600 PLEKHN1 FAM87B LOC100287934 FAM41C LOC100130417 LOC107985728 RNF223 LOC100288175 LINC00115 LOC105378947 HES4
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss TMEM240 LOC100288069 MIR6808 AURKAIP1 LINC01128 C1orf159 SSU72 KLHL17 SLC35E2 VWA1 MIR200B TTLL10-AS1 LOC102724312 NADK TNFRSF4 NOC2L MRPL20 ISG15 TTLL10 B3GALT6 CPTP MIR429 CCNL2 SAMD11 MIR6726 ACAP3 FAM87B TAS1R3 ATAD3B LOC100287934 ATAD3A LOC100130417 LOC107985728 CDK11B RNF223 LINC00115 HES4 LOC148413 ANKRD65 MIR200A PERM1 LOC105378948 UBE2J2 PUSL1 LINC01342 FNDC10 DVL1 MMP23B CPSF3L CDK11A TMEM88B ATAD3C SLC35E2B MIR6727 SCNN1D TNFRSF18 AGRN LOC107985729 SDF4 LOC284600 PLEKHN1 FAM132A FAM41C MIB2 MMP23A MXRA8 LOC100288175
dgv2n111 Chr.1:777165 - 877938 on Build GRCh38 Duplication FAM87B LOC100288069 LOC100287934 LINC01128 FAM41C LINC00115
dgv1n111 Chr.1:690090 - 939522 on Build GRCh38 Duplication LOC100288069 LINC01128 OR4F16 SAMD11 LOC107984841 LOC284600 FAM87B LOC100133331 LOC100287934 FAM41C LOC100130417 LOC107985728 LINC00115
nsv517709 Chr.1:817186 - 1275912 on Build GRCh38 Gain+Loss MIR200A PERM1 LINC01128 C1orf159 LOC105378948 UBE2J2 KLHL17 LINC01342 MIR200B TTLL10-AS1 TNFRSF4 NOC2L ISG15 TTLL10 B3GALT6 TNFRSF18 AGRN MIR429 SAMD11 SDF4 LOC284600 PLEKHN1 FAM132A FAM87B FAM41C LOC100130417 LOC107985728 RNF223 LOC100288175 LINC00115 HES4
nsv1159750 Chr.1:833413 - 883206 on Build GRCh38 Duplication LINC01128 FAM41C
dgv3n111 Chr.1:783283 - 939522 on Build GRCh38 Duplication FAM87B LOC100287934 LINC01128 FAM41C LOC100130417 LOC107985728 SAMD11 LINC00115 LOC284600
nsv832980 Chr.1:848279 - 1007037 on Build GRCh38 Gain NOC2L PERM1 LINC01128 FAM41C LOC100130417 LOC107985728 KLHL17 SAMD11 LOC284600 HES4 PLEKHN1
esv2762129 Chr.1:771719 - 901705 on Build GRCh38 Gain FAM87B LOC100288069 LOC100287934 LINC01128 FAM41C LINC00115
esv3584976 Chr.1:733250 - 914824 on Build GRCh38 Gain FAM87B LOC100288069 LOC100287934 LINC01128 FAM41C LINC00115 LOC107984841 LOC284600

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

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