IS30669 AND nstd71 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv901713	copy number variation	5	nstd71	human		NCBI36 chr14: 40,670,768-40,744,653 , GRCh37.p13 chr14: 41,601,018-41,674,903 , GRCh38.p12 chr14: 41,131,813-41,205,700	LINC02315
nsv880943	copy number variation	1	nstd71	human		NCBI36 chr5: 26,024,041-26,084,219 , GRCh37.p13 chr5: 25,988,284-26,048,462 , GRCh38.p12 chr5: 25,988,175-26,048,353	RNU4-43P
nsv880742	copy number variation	9	nstd71	human		NCBI36 chr4: 162,050,188-162,099,909 , GRCh37.p13 chr4: 161,830,738-161,880,459 , GRCh38.p12 chr4: 160,909,586-160,959,307	LOC105377513
nsv891046	copy number variation	2	nstd71	human		NCBI36 chr8: 78,427,867-78,474,370 , GRCh37.p13 chr8: 78,265,312-78,311,815 , GRCh38.p12 chr8: 77,353,076-77,399,579	LOC105375909
nsv887691	copy number variation	1	nstd71	human		NCBI36 chr7: 13,608,199-13,652,259 , GRCh37.p13 chr7: 13,641,674-13,685,734 , GRCh38.p12 chr7: 13,602,049-13,646,109	LOC107986770
nsv878763	copy number variation	13	nstd71	human		NCBI36 chr4: 25,163,609-25,192,329 , GRCh37.p13 chr4: 25,554,511-25,583,231 , GRCh38.p12 chr4: 25,552,889-25,581,609	LOC101929161
nsv900397	copy number variation	62	nstd71	human		NCBI36 chr13: 65,993,886-66,078,046 , GRCh37.p13 chr13: 67,095,885-67,180,045 , GRCh38.p12 chr13: 66,521,753-66,605,913	LOC105370247, PCDH9
nsv903637	copy number variation	11	nstd71	human		NCBI36 chr15: 21,975,505-22,036,253 , GRCh37.p13 chr15: 24,424,412-24,485,160 , GRCh38.p12 chr15: 24,179,265-24,240,013	LOC105370733, LOC105370732
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
nsv900152	copy number variation	33	nstd71	human		NCBI36 chr13: 56,638,784-56,698,642 , GRCh37.p13 chr13: 57,740,783-57,800,641 , GRCh38.p12 chr13: 57,166,649-57,226,507	MTCO2P3, LOC105370216, 2 more genes
nsv880849	copy number variation	9	nstd71	human		NCBI36 chr5: 592,310-659,384 , GRCh37.p13 chr5: 539,310-606,384 , GRCh38.p12 chr5: 539,195-606,269 , GRCh38.p12 chr5\|NT_187550.1: 20,628-89,376	CEP72-DT, LOC105374606, 2 more genes
nsv904012	copy number variation	1	nstd71	human		NCBI36 chr15: 32,481,609-32,631,865 , GRCh37.p13 chr15: 34,694,317-34,844,573 , GRCh38.p12 chr15: 34,402,116-34,552,372	GOLGA8A, HNRNPLP2, 5 more genes
nsv911533	copy number variation	1	nstd71	human		NCBI36 chr19: 32,553,835-32,757,923 , GRCh37.p13 chr19: 27,861,995-28,066,083 , GRCh38.p12 chr19: 27,371,087-27,575,175	0
nsv881457	copy number variation	4	nstd71	human		NCBI36 chr5: 17,642,680-17,766,033 , GRCh37.p13 chr5: 17,599,577-17,730,304 , GRCh38.p12 chr5: 17,599,468-17,730,195	H3Y1, H3P20, 4 more genes
nsv872210	copy number variation	1	nstd71	human		NCBI36 chr1: 143,328,536-143,636,149 , GRCh37.p13 chr1: 144,617,179-144,924,792 , GRCh38.p12 chr: NaN-NaN	0

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