2-1690-001 AND nstd173 - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4368029	copy number variation	55	nstd173	human		GRCh37 chr10: 68,077,579-68,122,519 , GRCh38.p12 chr10: 66,317,821-66,362,761	CTNNA3
nsv4387146	copy number variation	4	nstd173	human		GRCh37 chr6: 152,343,718-152,369,169 , GRCh38.p12 chr6: 152,022,583-152,048,034	ESR1
nsv4369980	copy number variation	1	nstd173	human		GRCh37 chr12: 84,028,783-84,457,826 , GRCh38.p12 chr12: 83,635,004-84,064,047	LOC107984536
nsv4383803	copy number variation	1	nstd173	human		GRCh37 chr11: 50,302,231-50,357,043 , GRCh38.p12 chr11: 50,343,060-50,397,872	LINC02750
nsv4372465	copy number variation	2	nstd173	human		GRCh37 chr5: 76,086,795-76,128,753 , GRCh38.p12 chr5: 76,790,970-76,832,928	F2RL1
nsv4374158	copy number variation	106	nstd173	human		GRCh37 chr3: 128,380,595-128,412,365 , GRCh38.p12 chr3: 128,661,752-128,693,522	POU5F1P6
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
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 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
nsv4368239	copy number variation	21	nstd173	human		GRCh37 chr6: 257,049-294,712 , GRCh38.p12 chr6: 257,049-294,712	, DUSP22, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4370840	copy number variation	154	nstd173	human		GRCh37 chr12: 11,222,368-11,247,388 , GRCh38.p12 chr12: 11,069,769-11,094,789	TAS2R43, TAS2R64P, 3 more genes
nsv4386828	copy number variation	67	nstd173	human		GRCh37 chr19: 20,596,118-20,716,388 , GRCh38.p12 chr19: 20,413,312-20,533,582	ZNF826P, ZNF737, 4 more genes
nsv4386552	copy number variation	30	nstd173	human		GRCh37 chr11: 54,701,512-54,788,759 , GRCh38.p12 chr11: 54,934,036-55,021,283	0
nsv4377501	copy number variation	53	nstd173	human		GRCh37 chrX: 115,133,416-115,156,164 , GRCh38.p12 chr: NaN-NaN	0

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