Hs03346553_cn

• Gene Symbol: FAM41C
• Assay Reference Genome Location: Chr.1:870226 on build GRCh38
• Cytoband: 1p36.33

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

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation