2-1189-001 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
nsv4367063	copy number variation	1	nstd173	human		GRCh37 chr21: 27,174,076-27,224,702 , GRCh38.p12 chr21: 25,801,765-25,852,391	LOC105372757
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
nsv4374667	copy number variation	4	nstd173	human		GRCh37 chr19: 41,360,130-41,392,641 , GRCh38.p12 chr19: 40,854,225-40,886,736	CYP2A7
nsv4369656	copy number variation	16	nstd173	human		GRCh37 chr5: 9,901,952-9,926,287 , GRCh38.p12 chr5: 9,901,840-9,926,175	LINC02112
nsv4368743	copy number variation	1	nstd173	human		GRCh37 chr3: 142,629,052-142,663,950 , GRCh38.p12 chr3: 142,910,210-142,945,108	LOC100507389
nsv4387002	copy number variation	71	nstd173	human		GRCh37 chr3: 128,380,595-128,412,377 , GRCh38.p12 chr3: 128,661,752-128,693,534	POU5F1P6
nsv4382158	copy number variation	11	nstd173	human		GRCh37 chr17: 44,187,492-44,212,428 , GRCh38.p12 chr17: 46,110,126-46,135,062 , GRCh38.p12 chr17\|NT_187663.1: 812,225-837,169	KANSL1
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
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
nsv4366808	copy number variation	2	nstd173	human		GRCh37 chrX: 148,688,249-148,738,858 , GRCh38.p12 chrX: 149,606,562-149,657,190	TMEM185A, LOC100420321
nsv4379472	copy number variation	106	nstd173	human		GRCh37 chr6: 257,061-294,923 , GRCh38.p12 chr6: 257,061-294,923	DUSP22, , 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
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 3 more genes
nsv4387935	copy number variation	6	nstd173	human		GRCh37 chr11: 51,337,076-51,377,164 , GRCh38.p12 chr11: 54,742,116-54,782,204	0
nsv4387125	copy number variation	432	nstd173	human		GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407	0
nsv4386306	copy number variation	141	nstd173	human		GRCh37 chrX: 924,088-944,608 , GRCh38.p12 chrX: 963,353-983,873	0
nsv4371527	copy number variation	186	nstd173	human		GRCh37 chr16: 34,449,595-34,755,828 , GRCh38.p12 chr16: 35,215,224-35,521,457	AGGF1P6, RARRES2P9, 27 more genes
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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