SP81243 AND nstd71 - dbVar - NCBI

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Items: 11

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Number of Variants: 11

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
nsv889264	copy number variation	16	nstd71	human		NCBI36 chr7: 141,410,335-141,447,476 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-243,158 , GRCh37.p13 chr7: 141,763,866-141,801,007 , GRCh38.p12 chr7\|NT_187562.1: 25,946-63,087 , GRCh38.p12 chr7: 142,064,066-142,101,207	MGAM
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
nsv902711	copy number variation	1	nstd71	human		NCBI36 chr15: 18,788,683-18,906,090 , GRCh37.p13 chr15: 20,528,669-20,646,076 , GRCh38.p12 chr15: 20,323,416-20,440,823	HERC2P3
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv882064	copy number variation	28	nstd71	human		NCBI36 chr5: 70,202,676-70,300,876 , GRCh37.p13 chr5: 70,166,920-70,265,120 , GRCh38.p12 chr5: 70,871,093-70,969,293	NAIP, SMN1, 3 more genes
nsv881885	copy number variation	26	nstd71	human		NCBI36 chr5: 69,345,138-69,436,209 , GRCh37.p13 chr5: 69,309,382-69,400,453 , GRCh38.p12 chr5\|NT_187651.1: 243,313-329,959 , GRCh38.p12 chr5: 70,013,555-70,104,626	SERF1B, GUSBP15, 3 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv896967	copy number variation	31	nstd71	human		NCBI36 chr11: 5,858,528-5,911,385 , GRCh37.p13 chr11: 5,901,952-5,954,809 , GRCh38.p12 chr11: 5,880,722-5,933,579	LOC112268071, OR52E4, 2 more genes
nsv902549	copy number variation	30	nstd71	human		NCBI36 chr14: 105,123,310-105,259,090 , GRCh37.p13 chr14\|NW_004166863.1: 249,095-384,875 , GRCh37.p13 chr14: 106,052,265-106,188,045 , GRCh38.p12 chr14: 105,605,043-105,721,708 , GRCh38.p12 chr14\|NT_187600.1: 72,812-189,477	IGHEP1, , 10 more genes
nsv884256	copy number variation	61	nstd71	human		NCBI36 chr6: 31,388,306-31,396,472 , GRCh37.p13 chr6: 31,280,327-31,288,493 , GRCh37.p13 chr6\|NT_167246.1: 2,627,146-2,631,393 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,622,207 , GRCh38.p12 chr6\|NT_167246.2: 2,621,526-2,625,775 , GRCh38.p12 chr6: 31,312,550-31,320,716 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,622,909	0

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