MS19503 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
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
nsv876330	copy number variation	1	nstd71	human		NCBI36 chr3: 1,251,092-1,275,820 , GRCh37.p13 chr3: 1,276,092-1,300,820 , GRCh38.p12 chr3: 1,234,408-1,259,136	CNTN6
nsv911749	copy number variation	35	nstd71	human		NCBI36 chr19: 46,044,103-46,075,668 , GRCh37.p13 chr19: 41,352,263-41,383,828 , GRCh38.p12 chr19: 40,846,358-40,877,923	CYP2A6, CYP2A7
nsv884021	copy number variation	25	nstd71	human		NCBI36 chr6: 30,034,633-30,045,903 , GRCh37.p13 chr6\|NT_167246.1: 1,225,247-1,236,501 , GRCh37.p13 chr6\|NT_167247.1: 1,308,516-1,319,775 , GRCh37.p13 chr6: 29,926,654-29,937,924 , GRCh38.p12 chr6\|NT_167247.2: 1,302,931-1,314,190 , GRCh38.p12 chr6\|NT_167246.2: 1,219,627-1,230,881 , GRCh38.p12 chr6: 29,958,877-29,970,147	HLA-W, MICD
nsv880475	copy number variation	143	nstd71	human		NCBI36 chr5: 32,137,157-32,205,304 , GRCh37.p13 chr5: 32,101,400-32,169,547 , GRCh38.p12 chr5: 32,101,294-32,169,441	PDZD2, GOLPH3
nsv887075	copy number variation	152	nstd71	human		NCBI36 chr7: 136,005-176,320 , GRCh37.p13 chr7: 40,922-81,237 , GRCh38.p12 chr7: 43,902-81,237 , GRCh38.p12 chr7\|NT_187558.1: 1-37,336 , GRCh38.p12 chr7\|NT_187653.1: 36,223-73,558	LOC101929756, LOC105375113
nsv911343	copy number variation	7	nstd71	human		NCBI36 chr19: 20,386,247-20,493,452 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-436,059 , GRCh37.p13 chr19: 20,522,409-20,701,612 , GRCh38.p12 chr19: 20,411,600-20,518,806	LOC105372317, BNIP3P23, 3 more genes
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
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
nsv879365	copy number variation	34	nstd71	human		NCBI36 chr4: 69,163,188-69,405,358 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv891427	copy number variation	2	nstd71	human		NCBI36 chr8: 122,480,530-122,541,478 , GRCh37.p13 chr8: 122,411,349-122,472,297 , GRCh38.p12 chr8: 121,399,109-121,460,057	0
nsv908527	copy number variation	11	nstd71	human		NCBI36 chr17: 41,863,070-41,922,658 , GRCh37.p13 chr17\|NT_167251.1: 263,369-308,670 , GRCh37.p13 chr17: 44,507,640-44,566,775 , GRCh38.p12 chr17: 46,444,391-46,489,976	0
nsv901768	copy number variation	1	nstd71	human		NCBI36 chr14: 42,555,382-42,600,039 , GRCh37.p13 chr14: 43,485,632-43,530,289 , GRCh38.p12 chr14: 43,016,429-43,061,086	0
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
nsv895272	copy number variation	10	nstd71	human		NCBI36 chr10: 47,013,541-47,454,088 , GRCh37.p13 chr10: 47,689,666-47,934,082 , GRCh38.p12 chr10: 46,172,299-46,398,663	AGAP14P, ANXA8L1, 6 more genes
nsv907812	copy number variation	60	nstd71	human		NCBI36 chr17: 18,865,850-19,040,640 , GRCh37.p13 chr17: 18,925,125-19,100,047 , GRCh38.p12 chr17: 19,021,812-19,196,734	SNORD3B-2, GRAPL, 11 more genes

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