SCOS_23 AND nstd53 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv869838	copy number variation	2	nstd53	human		GRCh38.p12 chr8: 15,555,657-15,584,588 , NCBI36 chr8: 15,457,537-15,486,468 , GRCh37.p13 chr8: 15,413,166-15,442,097	TUSC3
nsv870018	copy number variation	68	nstd53	human		NCBI36 chr20: 1,511,774-1,528,899 , GRCh37.p13 chr20: 1,563,774-1,580,899 , GRCh38.p12 chr20: 1,583,128-1,600,253	SIRPB1
nsv869630	copy number variation	1	nstd53	human		NCBI36 chr18: 57,185,169-57,220,672 , GRCh37.p13 chr18: 59,034,189-59,069,692 , GRCh38.p12 chr18: 61,366,956-61,402,459	CDH20, RNU6-116P
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
nsv870005	copy number variation	38	nstd53	human		NCBI36 chr12: 9,516,126-9,626,623 , GRCh38.p12 chr12: 9,472,263-9,582,760 , GRCh37.p13 chr12: 9,624,859-9,735,356	LOC408186, LOC100419520
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
nsv870249	copy number variation	4	nstd53	human		NCBI36 chr15: 18,854,127-20,393,586 , GRCh38.p12 chr15: 20,388,860-22,308,242 , GRCh37.p13 chr15: 20,594,113-22,842,145	NBEAP1, OR4H6P, 87 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
nsv869638	copy number variation	1	nstd53	human		NCBI36 chr5: 19,337,339-19,455,907 , GRCh37.p13 chr5: 19,301,582-19,420,150 , GRCh38.p12 chr5: 19,301,473-19,420,041	0
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
nsv870041	copy number variation	1	nstd53	human		GRCh37.p13 chr3: 197,710,951-197,840,264 , GRCh38.p12 chr3: 197,984,080-198,113,393 , NCBI36 chr3: 199,195,348-199,324,661	LMLN, ANKRD18DP, 4 more genes
nsv870034	copy number variation	4	nstd53	human		GRCh38.p12 chr10: 45,662,767-47,923,579 , NCBI36 chr10: 45,478,221-47,172,534 , GRCh37.p13 chr10: 46,158,215-47,702,528 , GRCh37.p13 chr10\|NW_003871068.1: 1-2,010,264	CTSLP2, GDF2, 72 more genes
nsv869958	copy number variation	83	nstd53	human		GRCh37.p13 chr3: 162,504,822-162,619,082 , GRCh38.p12 chr3: 162,787,034-162,901,294 , NCBI36 chr3: 163,987,516-164,101,776	0

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