Hs03383943_cn

• Gene Symbol: FAM87B
• Assay Reference Genome Location: Chr.1:817367 on build GRCh38
• Cytoband: 1p36.33

Target Gene Details

• Entrez Gene ID: 400728
• Gene Name: family with sequence similarity 87 member B
• Gene Aliases: -
• Location: Chr.1:817371-819834 on Build GRCh38
• Assay Gene Location: Overlaps - Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM87B	NR_103536.1
	AK097327.1			BAC04999.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv1004962	Chr.1:629241 - 915295 on Build GRCh38	Gain	LOC100133331 LINC01128 FAM87B FAM41C MTND1P23 MIR6723 LINC00115 MTND2P28 LOC284600 LOC100288069 LOC100287934 LOC107984841 OR4F16
esv3584977	Chr.1:777664 - 820586 on Build GRCh38	Loss	FAM87B LOC100288069 LOC100287934
nsv471522	Chr.1:586759 - 821403 on Build GRCh38	Gain	LOC105378947 LOC100133331 LOC101928626 MTND2P28 FAM87B MTND1P23 MIR6723 LOC100288069 LOC100287934 LOC107984841 OR4F16
nsv482937	Chr.1:10001 - 2368561 on Build GRCh38	Loss	GABRD RNF223 TMEM240 MTND2P28 MORN1 TTLL10 LOC107985728 TTLL10-AS1 LOC107985729 ATAD3A SSU72 LOC100132287 KLHL17 VWA1 MIR6723 ANKRD65 LOC105378591 LINC00115 PRKCZ TAS1R3 TMEM88B SLC35E2 LOC105378949 LINC01128 MMP23B LOC148413 LOC100506504 CCNL2 CDK11B C1orf159 LOC100130417 PERM1 LOC101928626 SAMD11 LOC105378592 MIR6859-1 LOC107984841 ATAD3B CPSF3L LOC100133331 LOC100134822 LOC105378948 FNDC10 CALML6 FAM132A MIR1302-2 NOC2L OR4F29 MIR6808 ISG15 MIR6859-2 CDK11A MIR6727 DDX11L1 OR4F16 MIR200B FAM41C FAAP20 ACAP3 PLEKHN1 MIR200A ATAD3C WASH7P CPTP FAM138A OR4F5 MTND1P23 LOC729737 SDF4 MRPL20 LOC100129534 GNB1 LOC100288175 MXRA8 FAM87B LOC105378589 CFAP74 MIR6726 TNFRSF4 PUSL1 UBE2J2 NADK TMEM52 LOC105378947 DVL1 SLC35E2B AURKAIP1 LOC102725121 MMP23A LOC100288069 TNFRSF18 AGRN SCNN1D LOC102724312 HES4 MIB2 MIR429 LOC284600 B3GALT6 LINC01342 LOC100287934 SKI
dgv1n67	Chr.1:811028 - 914557 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B FAM41C LOC284600
nsv1005935	Chr.1:805477 - 915295 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B FAM41C LOC284600
nsv10161	Chr.1:776731 - 1777210 on Build GRCh38	Gain+Loss	MIR200B FAM41C RNF223 ACAP3 TMEM240 PLEKHN1 MIR200A TTLL10 ATAD3C LOC107985728 TTLL10-AS1 LOC107985729 ATAD3A SSU72 CPTP KLHL17 VWA1 ANKRD65 SDF4 LINC00115 TAS1R3 MRPL20 TMEM88B SLC35E2 LOC100288175 MXRA8 LINC01128 FAM87B MMP23B MIR6726 LOC148413 TNFRSF4 CCNL2 PUSL1 UBE2J2 CDK11B NADK C1orf159 LOC100130417 PERM1 DVL1 SLC35E2B AURKAIP1 SAMD11 MMP23A LOC100288069 ATAD3B CPSF3L TNFRSF18 AGRN LOC105378948 SCNN1D FNDC10 LOC102724312 HES4 MIB2 MIR429 FAM132A NOC2L LOC284600 MIR6808 B3GALT6 ISG15 LINC01342 LOC100287934 CDK11A MIR6727
dgv5n100	Chr.1:585989 - 1114424 on Build GRCh38	Gain	LINC01128 FAM87B FAM41C RNF223 LOC105378947 C1orf159 LOC100130417 PERM1 LOC101928626 MTND2P28 PLEKHN1 SAMD11 LOC100288069 LOC107984841 LOC107985728 LOC100133331 AGRN KLHL17 LOC105378948 MTND1P23 MIR6723 HES4 LINC00115 NOC2L LOC284600 ISG15 LOC100287934 OR4F16 LOC100288175
dgv2n111	Chr.1:777165 - 877938 on Build GRCh38	Duplication	LINC00115 LINC01128 FAM87B FAM41C LOC100288069 LOC100287934
dgv1e55	Chr.1:817186 - 864083 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B
dgv1n111	Chr.1:690090 - 939522 on Build GRCh38	Duplication	LOC100133331 LINC01128 FAM87B FAM41C LINC00115 LOC100130417 SAMD11 LOC284600 LOC100288069 LOC100287934 LOC107984841 LOC107985728 OR4F16
nsv999785	Chr.1:771707 - 863579 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B LOC100288069 LOC100287934
dgv3n111	Chr.1:783283 - 939522 on Build GRCh38	Duplication	LINC00115 LOC100130417 LINC01128 FAM87B FAM41C SAMD11 LOC284600 LOC100287934 LOC107985728
nsv945734	Chr.1:803534 - 859995 on Build GRCh38	Duplication	LINC00115 LINC01128 FAM87B
esv2762129	Chr.1:771719 - 901705 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B FAM41C LOC100288069 LOC100287934
esv3584976	Chr.1:733250 - 914824 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B FAM41C LOC284600 LOC100288069 LOC100287934 LOC107984841
nsv1003571	Chr.1:629393 - 863579 on Build GRCh38	Loss	LINC00115 LOC100133331 LINC01128 MTND2P28 FAM87B MTND1P23 MIR6723 LOC100288069 LOC100287934 LOC107984841 OR4F16

More Information

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