MS13240 AND nstd71 - dbVar - NCBI

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Number of Variants: 18

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
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
nsv885314	copy number variation	24	nstd71	human		NCBI36 chr6: 32,632,202-32,647,375 , GRCh37.p13 chr6: 32,524,224-32,539,397 , GRCh38.p12 chr6: 32,556,447-32,571,620	HLA-DRB6
nsv886887	copy number variation	1	nstd71	human		NCBI36 chr6: 162,755,378-162,804,936 , GRCh37.p13 chr6: 162,835,388-162,884,946 , GRCh38.p12 chr6: 162,414,356-162,463,914	LOC105369171, PRKN
nsv895762	copy number variation	10	nstd71	human		NCBI36 chr10: 81,462,715-81,504,056 , GRCh37.p13 chr10: 81,472,521-81,513,880 , GRCh38.p12 chr10: 79,712,765-79,754,124	NUTM2B, NUTM2B-AS1
nsv902693	copy number variation	1	nstd71	human		NCBI36 chr15: 18,708,208-18,945,950 , GRCh37.p13 chr15: 20,448,194-20,685,936 , GRCh38.p12 chr15: 20,242,941-20,480,683	CHEK2P2, RHPN2P1, 1 more genes
nsv892765	copy number variation	2	nstd71	human		NCBI36 chr9: 22,695,094-22,837,961 , GRCh37.p13 chr9: 22,705,094-22,847,961 , GRCh38.p12 chr9: 22,705,095-22,847,962	LOC107987054, CLIC4P1, 1 more genes
nsv876271	copy number variation	1	nstd71	human		NCBI36 chr2: 242,591,551-242,645,262 , GRCh37.p13 chr2: 242,942,878-242,996,589 , GRCh38.p12 chr2: 242,000,727-242,054,438 , GRCh38.p12 chr2\|NT_187523.1: 39,422-98,508 , GRCh38.p12 chr2\|NT_187647.1: 39,422-98,148	LOC285097, LINC01237, 2 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv889306	copy number variation	1	nstd71	human		NCBI36 chr7: 143,028,896-143,126,726 , GRCh37.p13 chr7: 143,397,963-143,495,793 , GRCh38.p12 chr7: 143,700,870-143,798,700 , GRCh38.p12 chr7\|NW_018654714.1: 245,161-342,996	RPL26P24, , 4 more genes
nsv902787	copy number variation	16	nstd71	human		NCBI36 chr15: 19,031,743-19,558,265 , GRCh37.p13 chr15: 20,771,729-22,141,158 , GRCh38.p12 chr15: 20,566,406-21,498,353	, POTEB3, 39 more genes
nsv890161	copy number variation	90	nstd71	human		NCBI36 chr8: 7,242,915-7,459,302 , GRCh37.p13 chr8: 7,255,505-7,471,892 , GRCh38.p12 chr8\|NT_187570.1: 81,014-297,473 , GRCh38.p12 chr8: 7,397,983-7,614,370	FAM90A22, FAM90A21P, 17 more genes
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
nsv914711	copy number variation	52	nstd71	human		NCBI36 chr22: 23,991,725-24,254,444 , GRCh37.p13 chr22: 25,661,725-25,924,444 , GRCh38.p12 chr22: 25,265,758-25,528,477	LRP5L, MIR6817, 4 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
nsv901212	copy number variation	27	nstd71	human		NCBI36 chr14: 19,166,663-19,494,891 , GRCh37.p13 chr14: 20,096,940-20,425,051 , GRCh38.p12 chr14: 19,628,664-19,956,892	OR4K3, OR11K2P, 19 more genes
nsv875070	copy number variation	1	nstd71	human		NCBI36 chr2: 130,554,394-130,851,319 , GRCh37.p13 chr2: 130,837,924-131,134,849 , GRCh38.p12 chr2: 130,080,351-130,377,276	RNU6-1049P, CCDC115, 27 more genes
nsv903489	copy number variation	34	nstd71	human		NCBI36 chr15: 20,009,688-20,203,694 , GRCh37.p13 chr15: 22,508,324-22,652,330 , GRCh38.p12 chr: NaN-NaN	0

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