NA19101 AND nstd20 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438017	copy number variation	15	nstd20	human		NCBI34 chr8: 2,242,110-2,250,519 , GRCh37.p13 chr8\|NW_003571042.1: 289,314-297,723 , GRCh37.p13 chr8: 2,254,703-2,263,112 , GRCh38.p12 chr8\|NT_187576.1: 489,913-498,322	LOC105377783
nsv437939	copy number variation	19	nstd20	human		NCBI34 chr4: 138,551,715-138,556,685 , GRCh37.p13 chr4: 138,092,894-138,097,864 , GRCh38.p12 chr4: 137,171,740-137,176,710	LINC02511
nsv437905	copy number variation	6	nstd20	human		NCBI34 chr3: 192,388,157-192,390,897 , GRCh37.p13 chr3: 191,067,244-191,069,984 , GRCh38.p12 chr3: 191,349,455-191,352,195	CCDC50
nsv437922	copy number variation	25	nstd20	human		GRCh38.p12 chr4: 69,231,212-69,361,702 , GRCh37.p13 chr4: 70,096,930-70,227,420 , NCBI34 chr4: 70,412,475-70,542,965	UGT2B28, LOC642496, 2 more genes
nsv437894	copy number variation	301	nstd20	human		NCBI34 chr3: 163,826,348-163,943,569 , GRCh37.p13 chr3: 162,505,435-162,622,656 , GRCh38.p12 chr3: 162,787,647-162,904,868	0
nsv437910	copy number variation	98	nstd20	human		NCBI34 chr4: 9,969,524-9,998,131 , GRCh37.p13 chr4: 10,218,641-10,247,248 , GRCh38.p12 chr4: 10,217,017-10,245,624	0
nsv438214	copy number variation	10	nstd20	human		NCBI34 chr12: 57,502,971-57,518,064 , GRCh37.p13 chr12: 59,216,704-59,231,797 , GRCh38.p12 chr12: 58,822,922-58,838,015	0
nsv438192	copy number variation	2	nstd20	human		NCBI34 chr1: 12,541,839-12,549,327 , GRCh37.p13 chr1: 12,860,749-12,868,237 , GRCh38.p12 chr1: 12,800,601-12,808,101	0
nsv438005	copy number variation	72	nstd20	human		NCBI34 chr7: 125,601,054-125,603,762 , GRCh37.p13 chr7: 126,046,565-126,049,273 , GRCh38.p12 chr7: 126,406,511-126,409,219	0

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