SCOS_36 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
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
nsv869733	copy number variation	4	nstd53	human		NCBI36 chrX: 211,789-244,281 , GRCh37.p13 chrX: 291,789-324,281 , GRCh38.p12 chrX: 331,054-363,546 , GRCh38.p12 chrX\|NT_187667.1: 3,874-36,039 , GRCh38.p12 chrX\|NT_187634.1: 14,250-46,899	PPP2R3B
nsv869975	copy number variation	6	nstd53	human		NCBI36 chr18: 75,746,349-75,783,564 , GRCh37.p13 chr18: 77,645,361-77,682,576 , GRCh38.p12 chr18: 79,885,361-79,922,576	KCNG2, SLC66A2
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
nsv869807	copy number variation	87	nstd53	human		NCBI36 chr11: 55,118,273-55,200,744 , GRCh37.p13 chr11: 55,361,697-55,444,168 , GRCh38.p12 chr11: 55,594,221-55,676,692	OR4V1P, OR4P4, 3 more genes
nsv870269	copy number variation	4	nstd53	human		NCBI36 chr5: 523,621-546,203 , GRCh37.p13 chr5: 470,621-493,203 , GRCh38.p12 chr5: 470,506-493,088	SLC9A3, SLC9A3-OT1, 1 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
nsv870140	copy number variation	10	nstd53	human		GRCh37.p13 chr3: 195,340,900-195,454,454 , GRCh38.p12 chr3: 195,614,029-195,727,583 , NCBI36 chr3: 196,822,189-196,940,125 , GRCh38.p12 chr3\|NT_187649.1: 67,117-139,787 , GRCh38.p12 chr3\|NT_187688.1: 67,117-140,349 , GRCh38.p12 chr3\|NT_187690.1: 67,126-141,061 , GRCh38.p12 chr3\|NT_187691.1: 67,287-142,498 , GRCh38.p12 chr3\|NT_187678.1: 68,461-143,431 , GRCh38.p12 chr3\|NT_187689.1: 23,110-98,080 , GRCh38.p12 chr3\|NT_187532.1: 23,110-98,080	MUC20, MIR570HG, 9 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
nsv870333	copy number variation	7	nstd53	human		NCBI36 chr13: 68,138,971-68,158,986 , GRCh38.p12 chr13: 68,666,838-68,686,853 , GRCh37.p13 chr13: 69,240,970-69,260,985	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
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

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SCOS_36 AND nstd53 (15)
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