SP50775 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
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
nsv897084	copy number variation	3	nstd71	human		NCBI36 chr11: 24,189,180-24,265,500 , GRCh37.p13 chr11: 24,232,604-24,308,924 , GRCh38.p12 chr11: 24,211,058-24,287,378	LINC02686
nsv906026	copy number variation	11	nstd71	human		NCBI36 chr16: 32,413,490-32,579,320 , GRCh37.p13 chr16: 32,505,989-32,671,819 , GRCh38.p12 chr16: 32,494,668-32,660,498	FAM153DP, LOC107984013
nsv880606	copy number variation	1	nstd71	human		NCBI36 chr5: 35,071,336-35,120,937 , GRCh37.p13 chr5: 35,035,579-35,085,180 , GRCh38.p12 chr5: 35,035,474-35,085,078	AGXT2, PRLR
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
nsv885236	copy number variation	1	nstd71	human		NCBI36 chr6: 32,616,865-32,664,356 , GRCh37.p13 chr6: 32,508,887-32,556,378 , GRCh38.p12 chr6: 32,541,110-32,588,601	HLA-DRB6, RNU1-61P, 2 more genes
nsv873055	copy number variation	31	nstd71	human		NCBI36 chr1: 195,087,039-195,199,868 , GRCh37.p13 chr1: 196,820,416-196,933,245 , GRCh38.p12 chr1: 196,851,286-196,964,115	LOC105371675, LOC100996886, 2 more genes
nsv887576	copy number variation	7	nstd71	human		NCBI36 chr7: 10,015,056-10,062,801 , GRCh37.p13 chr7: 10,048,531-10,096,276 , GRCh38.p12 chr7: 10,008,904-10,056,649	0
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv897573	copy number variation	2	nstd71	human		NCBI36 chr11: 50,687,058-51,394,952 , GRCh37.p13 chr11: 50,730,482-51,538,376 , GRCh38.p12 chr: NaN-NaN	0

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