2-1508-001 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4387213	copy number variation	434	nstd173	human		GRCh37 chr4: 34,779,032-34,824,730 , GRCh38.p12 chr4: 34,777,410-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-315,437	LOC105378262
nsv4376255	copy number variation	343	nstd173	human		GRCh37 chr2: 98,118,199-98,162,176 , GRCh38.p12 chr2: 97,501,736-97,545,713	ANKRD36B
nsv4370897	copy number variation	108	nstd173	human		GRCh37 chr13: 57,758,269-57,778,367 , GRCh38.p12 chr13: 57,184,135-57,204,233	MTCO2P3
nsv4369227	copy number variation	203	nstd173	human		GRCh37 chr1: 72,771,366-72,811,904 , GRCh38.p12 chr1: 72,305,683-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,446	LOC105378797
nsv4375689	copy number variation	34	nstd173	human		GRCh37 chr20: 1,557,189-1,597,997 , GRCh38.p12 chr20: 1,576,543-1,617,351	SIRPB1
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
nsv4368509	copy number variation	1	nstd173	human		GRCh37 chr5: 7,413,808-7,473,837 , GRCh38.p12 chr5: 7,413,695-7,473,724	LOC105374646, ADCY2
nsv4366841	copy number variation	35	nstd173	human		GRCh37 chr1: 104,109,088-104,132,197 , GRCh38.p12 chr1: 103,566,466-103,589,575	ACTG1P4, AMY2B
nsv4369174	copy number variation	21	nstd173	human		GRCh37 chr2: 130,817,326-130,878,657 , GRCh38.p12 chr2: 130,059,753-130,121,084	POTEF, POTEF-AS1, 1 more genes
nsv4366629	copy number variation	16	nstd173	human		GRCh37 chr19: 54,730,238-54,753,327 , GRCh38.p12 chr19: 54,226,365-54,249,469 , GRCh38.p12 chr19\|NT_187693.1: 201,352-224,441 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-224,437 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-224,204	LILRA6, LOC100421130, 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
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4371560	copy number variation	26	nstd173	human		GRCh37 chr1: 248,637,251-248,795,289 , GRCh38.p12 chr1: 248,473,950-248,631,988	OR2T29, OR2T3, 9 more genes
nsv4379987	copy number variation	105	nstd173	human		GRCh37 chr14: 86,284,754-86,309,385 , GRCh38.p12 chr14: 85,818,410-85,843,041	0
nsv4369278	copy number variation	284	nstd173	human		GRCh37 chrX: 115,133,389-115,156,164 , GRCh38.p12 chr: NaN-NaN	0
nsv4387048	copy number variation	2	nstd173	human		GRCh37 chrX: 1,024,440-1,460,944 , GRCh38.p12 chrX: 1,063,705-1,342,051	, LOC652608, 9 more genes
nsv4367589	copy number variation	9	nstd173	human		GRCh37 chr11: 54,701,632-54,773,549 , GRCh38.p12 chr11: 54,934,156-55,006,073	0
nsv4381956	copy number variation	239	nstd173	human		GRCh37 chr5: 57,326,026-57,351,813 , GRCh38.p12 chr5: 58,030,199-58,055,986	0

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2-1508-001 AND nstd173 (19)
dbVar
PMC Articles for MedGen (Select 326914) (0)
PMC
LOC102725466 [Homo sapiens]
LOC102725466 [Homo sapiens]
Gene ID:102725466

Gene

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