OAT_20 AND nstd53 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv869745	copy number variation	1	nstd53	human		NCBI36 chr11: 91,114,713-91,253,132 , GRCh37.p13 chr11: 91,475,065-91,613,484 , GRCh38.p12 chr11: 91,741,899-91,880,318	LINC02756
nsv870374	copy number variation	79	nstd53	human		NCBI36 chr1: 72,541,502-72,589,682 , GRCh38.p12 chr1: 72,303,231-72,351,411 , GRCh37.p13 chr1: 72,768,914-72,817,094 , GRCh38.p12 chr1\|NW_018654707.1: 15,498-72,636	LOC105378797
nsv870002	copy number variation	49	nstd53	human		NCBI36 chr17: 41,527,764-41,566,540 , GRCh37.p13 chr17: 44,176,718-44,210,763 , GRCh38.p12 chr17: 46,094,581-46,133,397 , GRCh38.p12 chr17\|NT_187663.1: 796,687-835,504 , GRCh37.p13 chr17\|NT_167251.1: 655,282-689,337 , GRCh38.p12 chr17\|NT_167251.2: 653,289-691,821	KANSL1
nsv870256	copy number variation	7	nstd53	human		GRCh37.p13 chr3: 89,391,047-89,421,451 , GRCh38.p12 chr3: 89,341,897-89,372,301 , NCBI36 chr3: 89,473,737-89,504,141	EPHA3
nsv869729	copy number variation	57	nstd53	human		NCBI36 chr1: 150,823,126-150,848,509 , GRCh38.p12 chr1: 152,584,026-152,609,409 , GRCh37.p13 chr1: 152,556,502-152,581,885	LCE3C
nsv869990	copy number variation	71	nstd53	human		GRCh38.p12 chr6: 32,512,052-32,529,545 , NCBI36 chr6: 32,587,807-32,605,300 , GRCh37.p13 chr6: 32,479,829-32,497,322 , GRCh37.p13 chr6\|NT_167245.1: 3,821,149-3,834,945 , GRCh37.p13 chr6\|NT_167246.1: 3,995,584-4,009,378	HLA-DRB5
nsv869730	copy number variation	122	nstd53	human		GRCh38.p12 chr8: 39,377,532-39,528,580 , NCBI36 chr8: 39,354,208-39,505,256 , GRCh37.p13 chr8: 39,235,051-39,386,099	ADAM3A, ADAM5
nsv870129	copy number variation	3	nstd53	human		NCBI36 chr12: 19,361,719-19,476,466 , GRCh38.p12 chr12: 19,317,518-19,432,265 , GRCh37.p13 chr12: 19,470,452-19,585,199	PLEKHA5, AEBP2, 1 more genes
nsv870265	copy number variation	100	nstd53	human		NCBI36 chr22: 22,696,215-22,725,305 , GRCh37.p13 chr22: 24,366,215-24,395,305 , GRCh38.p12 chr22\|NT_187633.1: 260,390-289,480	GSTT1, LOC391322, 3 more genes
nsv870280	copy number variation	6	nstd53	human		NCBI36 chr14: 105,947,052-105,985,458 , GRCh38.p12 chr14: 106,420,093-106,458,490 , GRCh37.p13 chr14: 106,876,007-106,914,413 , GRCh38.p12 chr14\|NT_187600.1: 911,772-950,169 , GRCh37.p13 chr14\|NW_004166863.1: 1,083,260-1,121,657	IGH, IGHVII-40-1, 4 more genes
nsv870413	copy number variation	41	nstd53	human		GRCh38.p12 chr2: 34,472,710-34,513,110 , NCBI36 chr2: 34,551,281-34,591,681 , GRCh37.p13 chr2: 34,697,777-34,738,177	0
nsv869637	copy number variation	57	nstd53	human		NCBI36 chr14: 105,606,483-105,623,070 , GRCh37.p13 chr14: 106,535,438-106,552,025 , GRCh38.p12 chr: NaN-NaN	0
nsv870118	copy number variation	2	nstd53	human		NCBI36 chr14: 104,986,768-105,076,814 , GRCh38.p12 chr14: 105,449,386-105,533,002 , GRCh37.p13 chr14: 105,915,723-106,005,769 , GRCh37.p13 chr14\|NW_004166863.1: 112,553-202,599	CRIP1, CRIP2, 4 more genes
nsv870163	copy number variation	1	nstd53	human		NCBI36 chr7: 88,168,484-89,725,322 , GRCh37.p13 chr7: 88,330,548-89,887,386 , GRCh38.p12 chr7: 88,701,234-90,258,072	STEAP1, CFAP69, 10 more genes
nsv869925	copy number variation	6	nstd53	human		NCBI36 chr15: 19,109,183-19,805,960 , GRCh38.p12 chr15: 20,643,867-22,016,645 , GRCh37.p13 chr15: 20,849,169-22,304,596	NBEAP1, IGHD5OR15-5B, 60 more genes
nsv870440	copy number variation	38	nstd53	human		GRCh38.p12 chr8: 7,382,028-7,896,002 , NCBI36 chr8: 7,226,960-7,790,934 , GRCh37.p13 chr8: 7,239,550-7,753,524	DEFB4A, HSPD1P3, 41 more genes
nsv869782	copy number variation	92	nstd53	human		NCBI36 chr14: 19,273,348-19,478,367 , GRCh38.p12 chr14: 19,735,349-19,940,368 , GRCh37.p13 chr14: 20,203,508-20,408,527	OR4K6P, OR4K5, 10 more genes

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