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	LOC107984841 LOC284600 FAM41C LOC100133331 MTND2P28 OR4F16 MIR6723 MTND1P23 LINC00115 LINC01128 LOC100287934 LOC100288069 FAM87B
nsv471522	Chr.1:586759 - 821403 on Build GRCh38	Gain	LOC105378947 LOC107984841 MIR6723 MTND1P23 LOC101928626 LOC100133331 LOC100287934 MTND2P28 LOC100288069 OR4F16 FAM87B
esv3584978	Chr.1:777664 - 820586 on Build GRCh38	Gain	LOC100287934 LOC100288069 FAM87B
nsv482937	Chr.1:10001 - 2368561 on Build GRCh38	Loss	LOC100288175 ATAD3B MIR200A OR4F16 NADK MIR6723 LOC100132287 MXRA8 AURKAIP1 HES4 AGRN PERM1 NOC2L ATAD3A RNF223 LOC105378949 LOC105378589 WASH7P GNB1 LOC102724312 LOC148413 CALML6 LINC01128 SAMD11 LOC100506504 MMP23B TTLL10-AS1 TTLL10 SLC35E2 UBE2J2 CPTP LOC107985729 MIR6727 LOC100130417 LOC100287934 OR4F29 LOC107984841 SLC35E2B LOC107985728 TNFRSF4 MIR429 DDX11L1 CDK11B MORN1 ACAP3 DVL1 TAS1R3 OR4F5 LOC101928626 MIR6726 LOC100129534 FAM132A CCNL2 FAM87B LOC729737 VWA1 FAAP20 LOC100133331 PRKCZ TMEM88B LINC00115 ATAD3C TMEM240 MIR1302-2 PLEKHN1 LOC102725121 FAM138A TMEM52 MIR6859-2 FAM41C PUSL1 MTND2P28 MRPL20 MIR6808 LOC100134822 CFAP74 FNDC10 SKI MMP23A C1orf159 MIR200B TNFRSF18 GABRD KLHL17 LOC100288069 SSU72 LOC105378592 LOC105378947 LOC284600 MIR6859-1 SCNN1D CPSF3L LOC105378591 SDF4 ANKRD65 B3GALT6 MIB2 CDK11A ISG15 LOC105378948 MTND1P23 LINC01342
dgv1n67	Chr.1:811028 - 914557 on Build GRCh38	Gain	LOC284600 LINC00115 LINC01128 FAM41C FAM87B
nsv1005935	Chr.1:805477 - 915295 on Build GRCh38	Gain	LOC284600 LINC00115 LINC01128 FAM41C FAM87B
dgv5n100	Chr.1:585989 - 1114424 on Build GRCh38	Gain	LOC100288175 LOC100133331 KLHL17 OR4F16 MIR6723 LINC00115 LOC100130417 HES4 AGRN LOC100287934 PERM1 LOC100288069 LOC105378947 LOC107984841 PLEKHN1 NOC2L LOC284600 LOC107985728 RNF223 FAM41C MTND2P28 ISG15 LOC105378948 MTND1P23 LOC101928626 LINC01128 SAMD11 C1orf159 FAM87B
nsv10161	Chr.1:776731 - 1777210 on Build GRCh38	Gain+Loss	LOC100288175 VWA1 ATAD3B TMEM88B MIR200A NADK LINC00115 ATAD3C MXRA8 AURKAIP1 HES4 AGRN PERM1 TMEM240 PLEKHN1 NOC2L ATAD3A RNF223 FAM41C PUSL1 LOC102724312 MRPL20 LOC148413 MIR6808 LINC01128 FNDC10 SAMD11 MMP23A C1orf159 MMP23B MIR200B TTLL10-AS1 TTLL10 TNFRSF18 SLC35E2 UBE2J2 CPTP LOC107985729 KLHL17 MIR6727 LOC100130417 LOC100287934 LOC100288069 SSU72 SLC35E2B LOC284600 LOC107985728 SCNN1D TNFRSF4 CPSF3L MIR429 SDF4 ANKRD65 B3GALT6 MIB2 CDK11B ACAP3 CDK11A ISG15 LOC105378948 DVL1 TAS1R3 MIR6726 FAM132A CCNL2 LINC01342 FAM87B
dgv2n111	Chr.1:777165 - 877938 on Build GRCh38	Duplication	LINC00115 LINC01128 FAM41C LOC100287934 LOC100288069 FAM87B
nsv1159749	Chr.1:690090 - 833413 on Build GRCh38	Duplication	LOC107984841 LINC00115 LINC01128 LOC100133331 LOC100287934 LOC100288069 OR4F16 FAM87B
esv3890635	Chr.1:817186 - 848643 on Build GRCh38	Gain	LINC00115 LINC01128 FAM87B
nsv999785	Chr.1:771707 - 863579 on Build GRCh38	Gain	LINC00115 LINC01128 LOC100287934 LOC100288069 FAM87B
dgv3n111	Chr.1:783283 - 939522 on Build GRCh38	Duplication	LOC284600 LINC00115 LOC107985728 LINC01128 LOC100130417 FAM41C LOC100287934 SAMD11 FAM87B
nsv945734	Chr.1:803534 - 859995 on Build GRCh38	Duplication	LINC00115 LINC01128 FAM87B
esv2762129	Chr.1:771719 - 901705 on Build GRCh38	Gain	LINC00115 LINC01128 FAM41C LOC100287934 LOC100288069 FAM87B
nsv1003571	Chr.1:629393 - 863579 on Build GRCh38	Loss	LOC107984841 MIR6723 MTND1P23 LINC00115 LINC01128 LOC100133331 LOC100287934 MTND2P28 LOC100288069 OR4F16 FAM87B
esv3584976	Chr.1:733250 - 914824 on Build GRCh38	Gain	LOC107984841 LOC284600 LINC00115 LINC01128 FAM41C LOC100287934 LOC100288069 FAM87B

More Information

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