SP81354 AND nstd71 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv872693	copy number variation	223	nstd71	human		NCBI36 chr1: 187,587,641-187,815,034 , GRCh37.p13 chr1: 189,321,018-189,548,411 , GRCh38.p12 chr1: 189,351,888-189,579,281	LOC105371657
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
nsv881589	copy number variation	11	nstd71	human		NCBI36 chr4: 162,058,162-162,138,390 , GRCh37.p13 chr4: 161,838,712-161,918,940 , GRCh38.p12 chr4: 160,917,560-160,997,788	LOC105377513
nsv889863	copy number variation	1	nstd71	human		NCBI36 chr8: 2,329,741-2,383,995 , GRCh37.p13 chr8\|NW_003571042.1: 452,305-506,559 , GRCh37.p13 chr8: 2,342,334-2,396,588 , GRCh38.p12 chr8: 2,485,228-2,539,469 , GRCh38.p12 chr8\|NT_187576.1: 652,904-707,158	LINC03021
nsv897409	copy number variation	2	nstd71	human		NCBI36 chr11: 48,881,402-48,904,803 , GRCh37.p13 chr11: 48,924,826-48,948,227 , GRCh38.p12 chr11: 48,903,274-48,926,675	LOC100420449
nsv884192	copy number variation	4	nstd71	human		NCBI36 chr6: 31,384,589-31,392,232 , GRCh37.p13 chr6\|NT_167246.1: 2,623,436-2,631,067 , GRCh37.p13 chr6\|NT_167249.1: 2,610,355-2,617,963 , GRCh37.p13 chr6: 31,276,610-31,284,253 , GRCh38.p12 chr6: 31,308,833-31,316,476 , GRCh38.p12 chr6\|NT_167246.2: 2,617,816-2,625,447 , GRCh38.p12 chr6\|NT_167249.2: 2,611,057-2,618,665	LOC112267902
nsv890802	copy number variation	4	nstd71	human		NCBI36 chr8: 39,379,684-39,497,557 , GRCh37.p13 chr8: 39,260,527-39,378,400 , GRCh38.p12 chr8: 39,403,008-39,520,881	ADAM3A, ADAM5
nsv893244	copy number variation	4	nstd71	human		NCBI36 chr9: 43,599,125-43,677,629 , GRCh37.p13 chr9: 43,659,129-43,737,633 , GRCh38.p12 chr9: 42,076,756-42,155,260	LOC100420440, CNTNAP3B
nsv911382	copy number variation	222	nstd71	human		NCBI36 chr19: 20,413,668-20,520,617 , GRCh37.p13 chr19: 20,621,828-20,728,777 , GRCh37.p13 chr19\|NW_003571053.2: 356,275-463,224 , GRCh38.p12 chr19: 20,439,022-20,545,971	BNIP3P23, LOC105372317, 2 more genes
nsv893787	copy number variation	1	nstd71	human		NCBI36 chr9: 118,945,571-118,982,470 , GRCh37.p13 chr9: 119,905,750-119,942,649 , GRCh38.p12 chr9: 117,143,471-117,180,370	RPL10P3, SNORA70C, 1 more genes
nsv878668	copy number variation	1	nstd71	human		NCBI36 chr4: 9,160,192-9,260,511 , GRCh37.p13 chr4: 9,551,094-9,651,413 , GRCh38.p12 chr4: 9,549,473-9,649,789	RPS24P11, SNRPCP13, 2 more genes
nsv889773	copy number variation	3	nstd71	human		NCBI36 chr8: 2,118,593-2,201,720 , GRCh37.p13 chr8\|NW_003571042.1: 165,797-248,924 , GRCh37.p13 chr8: 2,131,186-2,214,313 , GRCh38.p12 chr8: 2,182,989-2,268,534 , GRCh38.p12 chr8\|NT_187576.1: 366,396-449,523	LOC105377782, LOC105377783, 2 more genes
nsv889328	copy number variation	1	nstd71	human		NCBI36 chr7: 143,088,653-143,206,916 , GRCh37.p13 chr7: 143,457,720-143,575,983 , GRCh38.p12 chr7\|NW_018654714.1: 304,948-423,114 , GRCh38.p12 chr7: 143,760,627-143,878,890	PAICSP6, TCAF2P1, 4 more genes
nsv889292	copy number variation	2	nstd71	human		NCBI36 chr7: 142,926,851-143,056,311 , GRCh37.p13 chr7: 143,216,729-143,425,378 , GRCh38.p12 chr7\|NW_018654714.1: 139,000-272,604 , GRCh38.p12 chr7: 143,519,636-143,728,285	EPHA1-AS1, CTAGE15, 8 more genes
nsv906024	copy number variation	73	nstd71	human		NCBI36 chr16: 32,413,490-32,511,911 , GRCh37.p13 chr16: 32,505,989-32,604,410 , GRCh38.p12 chr16: 32,494,668-32,593,089	0
nsv914607	copy number variation	103	nstd71	human		NCBI36 chr22: 22,600,777-22,713,954 , GRCh37.p13 chr22: 24,270,777-24,383,954 , GRCh38.p12 chr22\|NT_187633.1: 192,395-278,129	LOC100420769, DDT, 10 more genes

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