SP52552 AND nstd71 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

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
nsv897415	copy number variation	15	nstd71	human		NCBI36 chr11: 48,886,497-48,904,803 , GRCh37.p13 chr11: 48,929,921-48,948,227 , GRCh38.p12 chr11: 48,908,369-48,926,675	LOC100420449
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
nsv893228	copy number variation	16	nstd71	human		NCBI36 chr9: 43,570,503-43,730,292 , GRCh37.p13 chr9: 43,630,507-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,183,882	CNTNAP3B, LOC100420440, 1 more genes
nsv898666	copy number variation	8	nstd71	human		NCBI36 chr12: 7,884,583-7,990,569 , GRCh37.p13 chr12: 7,993,316-8,099,302 , GRCh38.p12 chr12: 7,840,720-7,946,706	NANOGP1, SLC2A14, 3 more genes
nsv909942	copy number variation	5	nstd71	human		NCBI36 chr18: 72,533,033-72,604,358 , GRCh37.p13 chr18: 74,404,045-74,475,370 , GRCh38.p12 chr18: 76,692,089-76,763,414	LINC01879, CCND3P2, 2 more genes
nsv879210	copy number variation	1	nstd71	human		NCBI36 chr4: 67,190,260-67,324,786 , GRCh37.p13 chr4: 67,507,665-67,642,191 , GRCh38.p12 chr4: 66,641,947-66,776,473	0
nsv909345	copy number variation	3	nstd71	human		NCBI36 chr18: 7,070,135-7,568,782 , GRCh37.p13 chr18: 7,080,135-7,578,782 , GRCh38.p12 chr18: 7,080,136-7,578,784	PTPRM, LRRC30, 7 more genes
nsv906527	copy number variation	1	nstd71	human		NCBI36 chr16: 33,090,901-33,214,305 , GRCh37.p13 chr16: 33,183,400-33,306,804 , GRCh38.p12 chr16: 33,172,079-33,504,337	LOC105379474, TP53TG3C, 6 more genes
nsv888867	copy number variation	1	nstd71	human		NCBI36 chr7: 101,970,902-102,126,404 , GRCh37.p13 chr7: 102,183,897-102,339,168 , GRCh38.p12 chr7: 102,543,450-102,698,721	UPK3BL1, POLR2J3, 6 more genes
nsv881457	copy number variation	4	nstd71	human		NCBI36 chr5: 17,642,680-17,766,033 , GRCh37.p13 chr5: 17,599,577-17,730,304 , GRCh38.p12 chr5: 17,599,468-17,730,195	H3Y1, H3P20, 4 more genes
nsv908127	copy number variation	14	nstd71	human		NCBI36 chr17: 31,462,326-31,889,664 , GRCh37.p13 chr17: 34,438,213-34,815,551 , GRCh37.p13 chr17\|NW_003315949.1: 68,401-344,487 , GRCh38.p12 chr17\|NT_187614.1: 345,741-694,641	, RN7SL301P, 18 more genes
nsv913395	copy number variation	5	nstd71	human		NCBI36 chr21: 14,153,631-14,197,852 , GRCh37.p13 chr21: 15,231,760-15,275,981 , GRCh38.p12 chr21: 13,859,439-13,903,660	0
nsv906473	copy number variation	1	nstd71	human		NCBI36 chr16: 32,475,644-32,494,598 , GRCh37.p13 chr16: 32,568,143-32,587,097 , GRCh38.p12 chr16: 32,556,822-32,575,776	0

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