SCOS_22 AND nstd53 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

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
nsv869764	copy number variation	1	nstd53	human		NCBI36 chr22: 28,653,649-28,697,813 , GRCh38.p12 chr22: 29,927,660-29,971,824 , GRCh37.p13 chr22: 30,323,649-30,367,813	MTMR3
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
nsv870244	copy number variation	26	nstd53	human		NCBI36 chr7: 141,408,072-141,438,504 , GRCh37.p13 chr7: 141,761,603-141,792,035 , GRCh38.p12 chr7: 142,061,803-142,092,235 , GRCh38.p12 chr7\|NT_187562.1: 23,683-54,115 , GRCh37.p13 chr7\|NW_003571040.1: 203,754-234,186	MGAM
nsv869833	copy number variation	2	nstd53	human		GRCh38.p12 chr4: 21,331,513-21,360,641 , GRCh37.p13 chr4: 21,333,136-21,362,264 , NCBI36 chr4: 20,942,234-20,971,362	KCNIP4
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
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
nsv869972	copy number variation	12	nstd53	human		NCBI36 chr12: 10,457,222-10,493,984 , GRCh38.p12 chr12: 10,413,356-10,450,118 , GRCh37.p13 chr12: 10,565,955-10,602,717	KLRC1, KLRC2, 1 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
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
nsv870346	copy number variation	5	nstd53	human		NCBI36 chr15: 32,530,060-32,664,506 , GRCh38.p12 chr15: 34,450,567-34,585,013 , GRCh37.p13 chr15: 34,742,768-34,877,214	FSCN1P1, GOLGA8B, 4 more genes
nsv869796	copy number variation	8	nstd53	human		GRCh38.p12 chr10: 46,157,935-47,923,579 , NCBI36 chr10: 46,399,331-47,021,415 , GRCh37.p13 chr10: 47,006,954-47,531,169 , GRCh37.p13 chr10\|NW_003871068.1: 431,049-2,010,264	CTSLP2, GDF2, 54 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
nsv870147	copy number variation	1	nstd53	human		NCBI36 chrX: 10,441-109,064 , GRCh37.p13 chrX: 70,441-169,064 , GRCh38.p12 chrX: 20,441-252,397	0
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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SCOS_22 AND nstd53 (17)
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