1-0901-004 AND nstd173 - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4375817	copy number variation	1	nstd173	human		GRCh37 chr14: 38,385,203-38,485,780 , GRCh38.p12 chr14: 37,915,998-38,016,575	LOC105370456
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4370761	copy number variation	67	nstd173	human		GRCh37 chr16: 55,796,388-55,822,431 , GRCh38.p12 chr16: 55,762,476-55,788,519	CES1P1
nsv4385079	copy number variation	34	nstd173	human		GRCh37 chr2: 98,141,300-98,162,176 , GRCh38.p12 chr2: 97,524,837-97,545,713	ANKRD36B
nsv4382709	copy number variation	1	nstd173	human		GRCh37 chr1: 48,212,615-48,480,271 , GRCh38.p12 chr1: 47,746,943-48,014,599	TRABD2B
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4369816	copy number variation	6	nstd173	human		GRCh37 chr15: 76,868,214-76,895,774 , GRCh38.p12 chr15: 76,575,873-76,603,433	SCAPER, MIR3713
nsv4383102	copy number variation	1	nstd173	human		GRCh37 chr19: 44,918,765-45,005,615 , GRCh38.p12 chr19: 44,414,596-44,501,563	ZNF180, ZNF229, 2 more genes
nsv4374702	copy number variation	95	nstd173	human		GRCh37 chr1: 1,616,990-1,672,603 , GRCh38.p12 chr1: 1,685,551-1,741,164	CDK11A, SLC35E2B, 3 more genes
nsv4383758	copy number variation	118	nstd173	human		GRCh37 chr4: 69,435,889-69,541,963 , GRCh38.p12 chr4: 68,570,171-68,676,245	LOC100422402, UGT2B17, 3 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4380030	copy number variation	42	nstd173	human		GRCh37 chr12: 11,219,995-11,247,388 , GRCh38.p12 chr12: 11,067,396-11,094,789	PRH1-PRR4, PRH1, 3 more genes
nsv4371422	copy number variation	21	nstd173	human		GRCh37 chr3: 162,521,309-162,651,027 , GRCh38.p12 chr3: 162,803,521-162,933,239	0
nsv4375821	copy number variation	11	nstd173	human		GRCh37 chr13: 89,796,612-89,837,548 , GRCh38.p12 chr13: 89,144,358-89,185,294	0
nsv4373369	copy number variation	7	nstd173	human		GRCh37 chr9: 32,100,686-32,127,551 , GRCh38.p12 chr9: 32,100,688-32,127,553	0
nsv4369278	copy number variation	284	nstd173	human		GRCh37 chrX: 115,133,389-115,156,164 , GRCh38.p12 chr: NaN-NaN	0
nsv4382296	copy number variation	16	nstd173	human		GRCh37 chr5: 180,374,898-180,442,428 , GRCh38.p12 chr5: 180,947,898-181,015,428	BTNL3, LOC100128762, 4 more genes
nsv4371070	copy number variation	6	nstd173	human		GRCh37 chr14: 22,760,452-22,960,757 , GRCh38.p12 chr14: 22,292,568-22,491,770	TRAJ51, TRDC, 32 more genes

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1-0901-004 AND nstd173 (20)
dbVar
PubChem Substance Links for Gene (Select 7755) (61)
PubChem Substance
Gene Links for GEO Profiles (Select 104012046) (0)
Gene
OMIM Links for GEO Profiles (Select 64946418) (1)
OMIM
NR2F2 nuclear receptor subfamily 2 group F member 2 [Homo sapiens]
NR2F2 nuclear receptor subfamily 2 group F member 2 [Homo sapiens]
Gene ID:7026

Gene

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