MS10098 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
nsv881656	copy number variation	1	nstd71	human	NCBI36 chr4: 179,225,142-179,292,610 , GRCh37.p13 chr4: 178,988,148-179,055,616 , GRCh38.p12 chr4: 178,066,994-178,134,462	RNU1-45P
nsv877861	copy number variation	1	nstd71	human	NCBI36 chr3: 165,384,881-165,451,319 , GRCh37.p13 chr3: 163,902,187-163,968,625 , GRCh38.p12 chr3: 164,184,399-164,250,837	LOC102724419
nsv908425	copy number variation	235	nstd71	human	NCBI36 chr17: 41,785,962-41,922,658 , GRCh37.p13 chr17: 44,430,206-44,566,775 , GRCh38.p12 chr17: 46,352,840-46,489,976	NSFP1, ARL17B
nsv872652	copy number variation	9	nstd71	human	NCBI36 chr1: 187,295,821-187,394,747 , GRCh37.p13 chr1: 189,029,198-189,128,124 , GRCh38.p12 chr1: 189,060,067-189,158,993	GAPDHP75, LOC105371657
nsv880475	copy number variation	143	nstd71	human	NCBI36 chr5: 32,137,157-32,205,304 , GRCh37.p13 chr5: 32,101,400-32,169,547 , GRCh38.p12 chr5: 32,101,294-32,169,441	PDZD2, GOLPH3
nsv879310	copy number variation	1929	nstd71	human	NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv883232	copy number variation	1	nstd71	human	NCBI36 chr5: 178,559,043-178,738,218 , GRCh37.p13 chr5: 178,626,437-178,805,612 , GRCh38.p12 chr5: 179,199,436-179,378,611 , GRCh38.p12 chr5\|NW_016107298.1: 1-143,318	LOC105377759, ADAMTS2, 1 more genes
nsv887589	copy number variation	1	nstd71	human	NCBI36 chr7: 10,275,485-10,440,930 , GRCh37.p13 chr7: 10,308,960-10,474,405 , GRCh38.p12 chr7: 10,269,333-10,434,778	0
nsv900716	copy number variation	1	nstd71	human	NCBI36 chr13: 84,426,033-84,512,475 , GRCh37.p13 chr13: 85,528,032-85,614,474 , GRCh38.p12 chr13: 84,953,897-85,040,339	0
nsv874423	copy number variation	2	nstd71	human	NCBI36 chr2: 83,081,762-83,154,608 , GRCh37.p13 chr2: 83,228,251-83,301,097 , GRCh38.p12 chr2: 83,001,127-83,073,973	0
nsv882586	copy number variation	4	nstd71	human	NCBI36 chr5: 104,498,285-104,570,387 , GRCh37.p13 chr5: 104,470,386-104,542,488 , GRCh38.p12 chr5: 105,134,685-105,206,787	0
nsv882276	copy number variation	2	nstd71	human	NCBI36 chr5: 84,227,950-84,299,468 , GRCh37.p13 chr5: 84,192,194-84,263,712 , GRCh38.p12 chr5: 84,896,376-84,967,894	0
nsv886378	copy number variation	1	nstd71	human	NCBI36 chr6: 94,979,558-95,028,478 , GRCh37.p13 chr6: 94,922,837-94,971,757 , GRCh38.p12 chr6: 94,213,119-94,262,039	0
nsv895538	copy number variation	101	nstd71	human	NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv884258	copy number variation	146	nstd71	human	NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv884620	copy number variation	1	nstd71	human	NCBI36 chr6: 32,065,343-32,119,296 , GRCh37.p13 chr6\|NT_167245.1: 3,242,946-3,270,782 , GRCh37.p13 chr6: 31,957,364-32,011,317 , GRCh37.p13 chr6\|NT_167247.1: 3,355,526-3,391,158 , GRCh37.p13 chr6\|NT_167249.1: 3,290,074-3,344,025 , GRCh38.p12 chr6: 31,989,587-32,043,540 , GRCh38.p12 chr6\|NT_167249.2: 3,290,776-3,344,727 , GRCh38.p12 chr6\|NT_167247.2: 3,349,941-3,385,573 , GRCh38.p12 chr6\|NT_167245.2: 3,237,361-3,265,197	C4A, STK19B, 7 more genes
nsv883625	copy number variation	2	nstd71	human	NCBI36 chr6: 29,963,685-30,005,175 , GRCh37.p13 chr6: 29,855,706-29,897,196 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,191,404 , GRCh38.p12 chr6: 29,887,929-29,929,419 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,185,784	HLA-H, HLA-A, 6 more genes
nsv903213	copy number variation	198	nstd71	human	NCBI36 chr15: 19,635,853-19,950,423 , GRCh37.p13 chr15: 21,371,194-22,449,059 , GRCh38.p12 chr15: 21,165,865-22,161,108	OR4H6P, OR4Q1P, 49 more genes
nsv874790	copy number variation	1	nstd71	human	NCBI36 chr2: 110,085,004-111,021,091 , GRCh37.p13 chr2: 110,727,715-111,334,482 , GRCh38.p12 chr2: 109,970,138-110,576,877	NPHP1, , 28 more genes
nsv882784	copy number variation	2	nstd71	human	NCBI36 chr5: 119,565,158-119,634,887 , GRCh37.p13 chr5: 119,537,259-119,606,988 , GRCh38.p12 chr5: 120,201,564-120,271,293	0

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Number of Variants: 20

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