SP51261 AND nstd71 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv886250	copy number variation	523	nstd71	human		NCBI36 chr6: 79,022,244-79,098,352 , GRCh37.p13 chr6: 78,965,525-79,041,633 , GRCh38.p12 chr6: 78,255,808-78,331,916	LOC105377865
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
nsv881222	copy number variation	185	nstd71	human		NCBI36 chr4: 162,058,162-162,152,452 , GRCh37.p13 chr4: 161,838,712-161,933,002 , GRCh38.p12 chr4: 160,917,560-161,011,850	LOC105377513
nsv901897	copy number variation	4	nstd71	human		NCBI36 chr14: 47,333,800-47,485,951 , GRCh37.p13 chr14: 48,264,050-48,416,201 , GRCh38.p12 chr14: 47,794,847-47,946,998	LOC100420098, LINC00648
nsv893124	copy number variation	1	nstd71	human		NCBI36 chr9: 40,516,952-40,658,850 , GRCh37.p13 chr9: 40,526,952-40,668,850 , GRCh38.p12 chr9: 67,023,991-67,165,889	CNTNAP3P2, USP12P3
nsv885417	copy number variation	5	nstd71	human		NCBI36 chr6: 32,639,901-32,666,924 , GRCh37.p13 chr6: 32,531,923-32,558,946 , GRCh38.p12 chr6: 32,564,146-32,591,169	RNU1-152P, HLA-DRB1
nsv912806	copy number variation	1	nstd71	human		NCBI36 chr20: 17,762,844-17,862,943 , GRCh37.p13 chr20: 17,814,844-17,914,943 , GRCh37.p13 chr20\|NW_003315966.1: 63,098-128,385 , GRCh38.p12 chr20\|NW_003315966.2: 63,098-128,386 , GRCh38.p12 chr20: 17,834,199-17,934,299	, RNU6-192P, 2 more genes
nsv890213	copy number variation	1	nstd71	human		NCBI36 chr8: 7,283,824-7,820,326 , GRCh37.p13 chr8: 7,296,414-7,782,916 , GRCh38.p12 chr8: 7,438,892-7,925,394	FAM90A23, FAM90A17, 38 more genes
nsv907824	copy number variation	10	nstd71	human		NCBI36 chr17: 18,886,060-19,040,640 , GRCh37.p13 chr17: 18,945,335-19,100,047 , GRCh38.p12 chr17: 19,042,022-19,196,734	SNORD3B-2, GRAPL, 10 more genes
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
nsv887001	copy number variation	155	nstd71	human		NCBI36 chr6: 169,246,516-169,271,889 , GRCh37.p13 chr6: 169,504,591-169,529,964 , GRCh38.p12 chr6: 169,104,496-169,129,869	0
nsv893241	copy number variation	23	nstd71	human		NCBI36 chr9: 43,594,114-44,683,090 , GRCh37.p13 chr9: 43,654,118-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	FGF7P4, MEP1AP4, 30 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

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SP51261 AND nstd71 (14)
dbVar
Iberian hop mosaic virus isolate SCR075-HluPRI-2014 large nuclear inclusion prot...
Iberian hop mosaic virus isolate SCR075-HluPRI-2014 large nuclear inclusion protein gene, partial cds
gi|1767854755|gb|MN531952.1|

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