SCOS_20 AND nstd53 - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
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
nsv869600	copy number variation	2	nstd53	human		NCBI36 chr1: 195,009,417-195,158,448 , GRCh38.p12 chr1: 196,773,664-196,922,695 , GRCh37.p13 chr1: 196,742,794-196,891,825	CFHR1, CFHR4, 3 more genes
nsv869708	copy number variation	1	nstd53	human		GRCh38.p12 chr2: 230,308,985-230,402,901 , NCBI36 chr2: 230,881,944-230,975,860 , GRCh37.p13 chr2: 231,173,700-231,267,616	SP140, SP140L, 1 more genes
nsv869717	copy number variation	4	nstd53	human		NCBI36 chr1: 246,812,484-246,878,405 , GRCh38.p12 chr1: 248,582,560-248,648,481 , GRCh37.p13 chr1: 248,745,861-248,811,782	OR2T10, OR2T11, 2 more genes
nsv870373	copy number variation	17	nstd53	human		NCBI36 chr12: 11,112,659-11,143,592 , GRCh38.p12 chr12: 11,068,793-11,099,726 , GRCh37.p13 chr12: 11,221,392-11,252,325	PRH1, TAS2R43, 3 more genes
nsv870291	copy number variation	3	nstd53	human		NCBI36 chr16: 21,258,078-21,501,073 , GRCh38.p12 chr16: 21,339,256-21,582,251 , GRCh37.p13 chr16: 21,350,577-21,593,572	NPIPB3, SLC7A5P2, 5 more genes
nsv869711	copy number variation	90	nstd53	human		NCBI36 chr4: 69,099,876-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv870032	copy number variation	7	nstd53	human		NCBI36 chrX: 16,054-85,768 , GRCh37.p13 chrX: 76,054-145,768 , GRCh38.p12 chrX: 26,054-229,101	0
nsv870121	copy number variation	1	nstd53	human		GRCh37.p13 chr3: 2,665,466-3,679,126 , GRCh38.p12 chr3: 2,623,782-3,637,442 , NCBI36 chr3: 2,640,466-3,654,126	IL5RA, TRNT1, 5 more genes
nsv869591	copy number variation	3	nstd53	human		NCBI36 chr16: 33,348,570-33,559,207 , GRCh38.p12 chr16: 33,638,602-33,849,239 , GRCh37.p13 chr16: 33,441,069-33,651,706	IGHV3OR16-12, LOC342443, 7 more genes
nsv869957	copy number variation	1	nstd53	human		NCBI36 chr14: 105,597,311-106,013,552 , GRCh38.p12 chr14: 106,070,018-106,486,500 , GRCh37.p13 chr14: 106,526,266-106,942,507 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	IGH, IGHVIV-44-1, 113 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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SCOS_20 AND nstd53 (14)
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