2-1330-001 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
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
nsv4382387	copy number variation	7	nstd173	human		GRCh37 chr16: 55,796,376-55,821,956 , GRCh38.p12 chr16: 55,762,464-55,788,044	CES1P1
nsv4381490	copy number variation	65	nstd173	human		GRCh37 chr3: 89,394,591-89,419,375 , GRCh38.p12 chr3: 89,345,441-89,370,225	EPHA3
nsv4375513	copy number variation	189	nstd173	human		GRCh37 chr1: 72,771,354-72,812,440 , GRCh38.p12 chr1: 72,305,671-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,938-67,982	LOC105378797
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
nsv4370274	copy number variation	9	nstd173	human		GRCh37 chr12: 11,503,225-11,553,861 , GRCh38.p12 chr12: 11,350,291-11,400,927 , GRCh38.p12 chr12\|NT_187658.1: 545,254-572,349	PRB2, PRB1
nsv4368683	copy number variation	3	nstd173	human		GRCh37 chr19: 41,356,472-41,385,370 , GRCh38.p12 chr19: 40,850,567-40,879,465	CYP2A6, CYP2A7
nsv4376723	copy number variation	40	nstd173	human		GRCh37 chr12: 8,558,475-8,584,702 , GRCh38.p12 chr12: 8,405,879-8,432,106	OR7E140P, OR7E148P
nsv4371574	copy number variation	3	nstd173	human		GRCh37 chr6: 254,254-381,148 , GRCh38.p12 chr6: 254,254-381,148	, , 1 more genes
nsv4379956	copy number variation	132	nstd173	human		GRCh37 chr17: 44,212,824-44,292,754 , GRCh38.p12 chr17: 46,135,458-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,565-917,561	LOC107985027, KANSL1, 1 more genes
nsv4381404	copy number variation	4	nstd173	human		GRCh37 chr17: 19,499,735-19,538,758 , GRCh38.p12 chr17: 19,596,422-19,635,445	SLC47A1P1, MTCO1P39, 3 more genes
nsv4375662	copy number variation	272	nstd173	human		GRCh37 chr11: 5,783,910-5,809,230 , GRCh38.p12 chr11: 5,762,680-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 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
nsv4372679	copy number variation	125	nstd173	human		GRCh37 chr14: 74,001,111-74,029,899 , GRCh38.p12 chr14: 73,534,407-73,563,195	HEATR4, ACOT1, 1 more genes
nsv4368012	copy number variation	4	nstd173	human		GRCh37 chr17: 36,283,807-36,410,533 , GRCh38.p12 chr17\|NT_187614.1: 2,162,872-2,289,598	NPEPPSP1, TBC1D3, 6 more genes
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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