IS32653 AND nstd71 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv909309	copy number variation	3	nstd71	human	NCBI36 chr18: 1,710,627-1,855,220 , GRCh37.p13 chr18: 1,720,627-1,865,220 , GRCh38.p12 chr18: 1,720,626-1,865,219 , GRCh38.p12 chr18\|NW_019805503.1: 1-143,568	LOC105371959
nsv882591	copy number variation	9	nstd71	human	NCBI36 chr5: 104,498,285-104,624,389 , GRCh37.p13 chr5: 104,470,386-104,596,490 , GRCh38.p12 chr5: 105,134,685-105,260,789	LOC105379110
nsv871494	copy number variation	4	nstd71	human	NCBI36 chr1: 103,126,726-103,239,505 , GRCh37.p13 chr1: 103,354,138-103,466,917 , GRCh38.p12 chr1: 102,888,582-103,001,361	COL11A1
nsv891308	copy number variation	12	nstd71	human	NCBI36 chr8: 112,141,166-112,232,977 , GRCh37.p13 chr8: 112,071,990-112,163,801 , GRCh38.p12 chr8: 111,059,761-111,151,572	LINC01609
nsv887677	copy number variation	4	nstd71	human	NCBI36 chr7: 13,355,193-13,433,727 , GRCh37.p13 chr7: 13,388,668-13,467,202 , GRCh38.p12 chr7: 13,349,043-13,427,577	LOC107986770
nsv886178	copy number variation	16	nstd71	human	NCBI36 chr6: 75,596,154-75,667,442 , GRCh37.p13 chr6: 75,539,434-75,610,722 , GRCh38.p12 chr6: 74,829,718-74,901,006	NUP50P4
nsv884832	copy number variation	107	nstd71	human	NCBI36 chr6: 32,560,168-32,601,256 , GRCh37.p13 chr6: 32,452,190-32,493,278 , GRCh38.p12 chr6: 32,484,413-32,525,501	HLA-DRB5
nsv909830	copy number variation	31	nstd71	human	NCBI36 chr18: 64,890,061-64,909,808 , GRCh37.p13 chr18: 66,739,081-66,758,828 , GRCh38.p12 chr18: 69,071,844-69,091,591	CCDC102B
nsv908938	copy number variation	2	nstd71	human	NCBI36 chr17: 74,878,104-74,905,632 , GRCh37.p13 chr17: 77,366,509-77,394,037 , GRCh38.p12 chr17: 79,370,427-79,397,955	RBFOX3
nsv885690	copy number variation	1	nstd71	human	NCBI36 chr6: 32,776,824-32,782,627 , GRCh37.p13 chr6\|NT_167247.1: 4,005,905-4,011,696 , GRCh37.p13 chr6\|NT_167245.1: 3,951,270-3,957,061 , GRCh37.p13 chr6: 32,668,846-32,674,649 , GRCh37.p13 chr6\|NT_167249.1: 4,100,987-4,106,800 , GRCh38.p12 chr6\|NT_167245.2: 3,945,685-3,951,476 , GRCh38.p12 chr6: 32,701,069-32,706,872 , GRCh38.p12 chr6\|NT_167249.2: 4,101,689-4,107,502 , GRCh38.p12 chr6\|NT_167247.2: 4,000,320-4,006,111	MTCO3P1
nsv912879	copy number variation	1	nstd71	human	NCBI36 chr20: 40,662,631-40,719,392 , GRCh37.p13 chr20: 41,229,217-41,285,978 , GRCh38.p12 chr20: 42,600,577-42,657,338	PTPRT, LOC105372624
nsv898873	copy number variation	29	nstd71	human	NCBI36 chr12: 20,899,271-20,907,027 , GRCh37.p13 chr12: 21,008,004-21,015,760 , GRCh38.p12 chr12: 20,855,070-20,862,826	SLCO1B3-SLCO1B7, SLCO1B3
nsv904408	copy number variation	1	nstd71	human	NCBI36 chr15: 74,671,182-74,872,338 , GRCh37.p13 chr15: 76,884,127-77,085,283 , GRCh38.p12 chr15: 76,591,786-76,792,942	SCAPER, RN7SKP217
nsv875504	copy number variation	3	nstd71	human	NCBI36 chr2: 184,951,101-184,992,674 , GRCh37.p13 chr2: 185,242,856-185,284,429 , GRCh38.p12 chr2: 184,378,129-184,419,702	MIR548AE1, LOC105373776, 2 more genes
nsv878234	copy number variation	1	nstd71	human	NCBI36 chr4: 47,538-157,596 , GRCh37.p13 chr4\|NW_004775427.1: 47,645-156,858 , GRCh37.p13 chr4: 57,538-160,647 , GRCh38.p12 chr4: 57,645-173,807	ZNF718, WEE1P1, 1 more genes
nsv876265	copy number variation	70	nstd71	human	NCBI36 chr2: 242,429,063-242,692,820 , GRCh37.p13 chr2: 242,780,390-243,044,147 , GRCh38.p12 chr2: 241,838,238-242,101,996 , GRCh38.p12 chr2\|NT_187523.1: 1-146,066 , GRCh38.p12 chr2\|NT_187647.1: 1-145,706	LINC01881, LINC01237, 9 more genes
nsv889109	copy number variation	134	nstd71	human	NCBI36 chr7: 118,855,366-118,964,906 , GRCh37.p13 chr7: 119,068,130-119,177,670 , GRCh38.p12 chr7: 119,428,076-119,537,616	0
nsv880018	copy number variation	2	nstd71	human	NCBI36 chr4: 133,396,347-133,498,363 , GRCh37.p13 chr4: 133,176,897-133,278,913 , GRCh38.p12 chr4: 132,255,742-132,357,758	0
nsv903249	copy number variation	2	nstd71	human	NCBI36 chr15: 19,635,853-20,249,841 , GRCh37.p13 chr15: 21,371,194-22,698,477 , GRCh38.p12 chr15: 21,165,865-22,308,242	IGHV1OR15-1, GRAMD4P6, 56 more genes
nsv902785	copy number variation	8	nstd71	human	NCBI36 chr15: 19,031,743-19,541,911 , GRCh37.p13 chr15: 20,771,729-22,141,158 , GRCh38.p12 chr15: 20,566,406-21,498,353	VN1R60P, SPATA31E2P, 39 more genes

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Number of Variants: 20

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