SP50766 AND nstd71 - dbVar - NCBI

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Items: 17

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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
nsv884852	copy number variation	234	nstd71	human		NCBI36 chr6: 32,561,832-32,593,470 , GRCh37.p13 chr6: 32,453,854-32,485,492 , GRCh38.p12 chr6: 32,486,077-32,517,715	HLA-DRB5
nsv889507	copy number variation	10	nstd71	human		NCBI36 chr7: 152,226,785-152,251,305 , GRCh37.p13 chr7: 152,595,852-152,620,372 , GRCh38.p12 chr7: 152,898,767-152,923,287	ACTR3B
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
nsv872974	copy number variation	1	nstd71	human		NCBI36 chr1: 194,923,360-194,929,082 , GRCh37.p13 chr1: 196,656,737-196,662,459 , GRCh38.p12 chr1: 196,687,607-196,693,329	CFH
nsv879350	copy number variation	13	nstd71	human		NCBI36 chr4: 69,127,630-69,163,108 , GRCh37.p13 chr4: 69,445,035-69,480,513 , GRCh38.p12 chr4: 68,579,317-68,614,795	LOC100422402, LOC100132651
nsv893265	copy number variation	25	nstd71	human		NCBI36 chr9: 43,609,749-43,730,292 , GRCh37.p13 chr9: 43,669,753-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,144,636	CNTNAP3B, LOC100420440
nsv908557	copy number variation	103	nstd71	human		NCBI36 chr17: 42,005,250-42,143,493 , GRCh37.p13 chr17: 44,649,934-44,788,310 , GRCh38.p12 chr17: 46,572,568-46,710,944	NSF, LRRC37A2, 1 more genes
nsv874657	copy number variation	2	nstd71	human		NCBI36 chr2: 89,949,717-91,012,753 , GRCh37.p13 chr2: 90,312,412-91,649,026 , GRCh38.p12 chr2: 90,273,552-91,456,652	IGKV1OR2-118, LOC101926946
nsv903499	copy number variation	1	nstd71	human		NCBI36 chr15: 20,288,320-20,532,408 , GRCh37.p13 chr15: 22,736,956-22,980,967 , GRCh38.p12 chr15: 22,892,101-23,136,112 , GRCh38.p12 chr15\|NT_187603.1: 1-236,620	GOLGA6L1, LOC101060118, 3 more genes
nsv908379	copy number variation	346	nstd71	human		NCBI36 chr17: 41,775,690-41,922,658 , GRCh37.p13 chr17: 44,419,932-44,566,775 , GRCh38.p12 chr17: 46,342,566-46,489,976	ARL17B, NSFP1, 1 more genes
nsv895040	copy number variation	18	nstd71	human		NCBI36 chr10: 38,740,240-38,781,106 , GRCh37.p13 chr10: 38,700,234-38,741,100 , GRCh38.p12 chr10: 38,411,306-38,452,172	LINC00999, LOC101929540, 2 more genes
nsv873954	copy number variation	7	nstd71	human		NCBI36 chr2: 41,360,563-41,436,748 , GRCh37.p13 chr2: 41,507,059-41,583,244 , GRCh38.p12 chr2: 41,279,919-41,356,104	0
nsv913323	copy number variation	11	nstd71	human		NCBI36 chr21: 1-9,876,943 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv903567	copy number variation	1	nstd71	human		NCBI36 chr15: 20,551,298-20,796,527 , GRCh37.p13 chr15: 22,999,857-23,245,086 , GRCh38.p12 chr15: 22,628,010-22,873,211	NIPA2, LOC283683, 8 more genes
nsv880294	copy number variation	63	nstd71	human		NCBI36 chr4: 162,075,534-162,151,909 , GRCh37.p13 chr4: 161,856,084-161,932,459 , GRCh38.p12 chr4: 160,934,932-161,011,307	0
nsv897377	copy number variation	19	nstd71	human		NCBI36 chr11: 48,680,611-48,749,266 , GRCh37.p13 chr11: 48,724,035-48,792,690 , GRCh38.p12 chr11: 48,702,483-48,771,138	0
nsv906637	copy number variation	60	nstd71	human		NCBI36 chr16: 33,778,130-33,819,975 , GRCh37.p13 chr16: 33,870,629-33,912,474 , GRCh38.p12 chr16: 34,068,162-34,110,007	0

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