MS22998 AND nstd71 - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv881519	copy number variation	38	nstd71	human		NCBI36 chr4: 178,201,142-178,397,447 , GRCh37.p13 chr4: 177,964,148-178,160,453 , GRCh38.p12 chr4: 177,042,994-177,239,299	LOC105377557, RN7SKP136
nsv881673	copy number variation	95	nstd71	human		NCBI36 chr5: 9,953,083-9,981,862 , GRCh37.p13 chr5: 9,900,083-9,928,862 , GRCh38.p12 chr5: 9,899,971-9,928,750	LOC107986405, LINC02112
nsv905854	copy number variation	8	nstd71	human		NCBI36 chr16: 32,359,228-32,511,911 , GRCh37.p13 chr16: 32,451,727-32,604,410 , GRCh38.p12 chr16: 32,440,406-32,593,089	ABCD1P3, PABPC1P13
nsv895761	copy number variation	319	nstd71	human		NCBI36 chr10: 81,462,715-81,497,813 , GRCh37.p13 chr10: 81,472,521-81,507,631 , GRCh38.p12 chr10: 79,712,765-79,747,875	NUTM2B, NUTM2B-AS1
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
nsv880162	copy number variation	1	nstd71	human		NCBI36 chr4: 140,771,849-140,831,509 , GRCh37.p13 chr4: 140,552,399-140,612,059 , GRCh38.p12 chr4: 139,631,245-139,690,905	MGST2, RN7SKP237, 1 more genes
nsv885041	copy number variation	15	nstd71	human		NCBI36 chr6: 32,604,890-32,639,223 , GRCh37.p13 chr6: 32,496,912-32,531,245 , GRCh38.p12 chr6: 32,529,135-32,563,468	HLA-DRB5, HLA-DRB6, 1 more genes
nsv883570	copy number variation	167	nstd71	human		NCBI36 chr6: 29,957,666-29,972,182 , GRCh37.p13 chr6: 29,849,687-29,864,203 , GRCh38.p12 chr6: 29,881,910-29,896,426	HLA-T, HCG4P7, 1 more genes
nsv883782	copy number variation	2	nstd71	human		NCBI36 chr6: 29,976,032-30,005,175 , GRCh37.p13 chr6\|NT_167246.1: 1,162,230-1,191,404 , GRCh37.p13 chr6: 29,868,053-29,897,196 , GRCh38.p12 chr6\|NT_167246.2: 1,156,610-1,185,784 , GRCh38.p12 chr6: 29,900,276-29,929,419	HCG4B, HLA-K, 4 more genes
nsv895213	copy number variation	2	nstd71	human		NCBI36 chr10: 46,803,075-47,197,303 , GRCh37.p13 chr10: 47,529,170-47,727,297 , GRCh38.p12 chr: NaN-NaN	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
nsv880709	copy number variation	4	nstd71	human		NCBI36 chr4: 187,166,640-187,368,378 , GRCh37.p13 chr4: 186,929,646-187,131,384 , GRCh38.p12 chr4: 186,008,492-186,210,230	TLR3, FLJ38576, 5 more genes
nsv901367	copy number variation	1	nstd71	human		NCBI36 chr14: 19,294,807-19,515,210 , GRCh37.p13 chr14: 20,224,967-20,445,370 , GRCh38.p12 chr14: 19,756,808-19,977,211	OR4N1P, LOC100421751, 11 more genes
nsv882258	copy number variation	11	nstd71	human		NCBI36 chr5: 84,039,445-84,156,824 , GRCh37.p13 chr5: 84,003,689-84,121,068 , GRCh38.p12 chr5: 84,707,871-84,825,250	0
nsv885656	copy number variation	20	nstd71	human		NCBI36 chr6: 32,746,293-32,765,312 , GRCh37.p13 chr6\|NT_167247.1: 3,972,621-3,985,429 , GRCh37.p13 chr6: 32,638,315-32,657,334 , GRCh38.p12 chr6: 32,670,538-32,689,557 , GRCh38.p12 chr6\|NT_167247.2: 3,967,036-3,979,844	0

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MS22998 AND nstd71 (18)
dbVar
GSM7103649[Accession] (3)
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