NA18542 AND nstd20 - dbVar - NCBI

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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
nsv437907	copy number variation	146	nstd20	human		NCBI34 chr3: 194,196,286-194,205,086 , GRCh37.p13 chr3: 192,875,373-192,884,173 , GRCh38.p12 chr3: 193,157,584-193,166,384	VEZF1P1
nsv438378	copy number variation	12	nstd20	human		NCBI34 chr2: 196,183,303-196,184,993 , GRCh37.p13 chr2: 195,980,760-195,982,450 , GRCh38.p12 chr2: 195,116,036-195,117,726	LOC105376755
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
nsv438337	copy number variation	50	nstd20	human		NCBI34 chr2: 52,726,065-52,757,084 , GRCh37.p13 chr2: 52,751,531-52,782,550 , GRCh38.p12 chr2: 52,524,393-52,555,412	0
nsv437920	copy number variation	29	nstd20	human		NCBI34 chr4: 64,701,164-64,713,008 , GRCh37.p13 chr4: 64,697,784-64,709,628 , GRCh38.p12 chr4: 63,832,066-63,843,910	0
nsv438371	copy number variation	55	nstd20	human		NCBI34 chr2: 147,075,728-147,086,685 , GRCh37.p13 chr2: 146,864,959-146,875,916 , GRCh38.p12 chr2: 146,107,391-146,118,348	0
nsv437919	copy number variation	22	nstd20	human		NCBI34 chr4: 63,672,955-63,678,558 , GRCh37.p13 chr4: 63,669,575-63,675,178 , GRCh38.p12 chr4: 62,803,857-62,809,460	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
nsv438352	copy number variation	3	nstd20	human		NCBI34 chr2: 59,598,122-59,600,156 , GRCh37.p13 chr2: 59,623,588-59,625,622 , GRCh38.p12 chr2: 59,396,453-59,398,487	0

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