SP51172 AND nstd71 - dbVar - NCBI

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv890784	copy number variation	129	nstd71	human		NCBI36 chr8: 39,356,825-39,509,376 , GRCh37.p13 chr8: 39,237,668-39,390,219 , GRCh38.p12 chr8: 39,380,149-39,532,700	ADAM3A, ADAM5
nsv900176	copy number variation	2	nstd71	human		NCBI36 chr13: 56,659,853-56,725,158 , GRCh37.p13 chr13: 57,761,852-57,827,157 , GRCh38.p12 chr13: 57,187,718-57,253,023	LOC105370216, MTCO2P3
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
nsv882365	copy number variation	1	nstd71	human		NCBI36 chr5: 89,806,524-89,918,374 , GRCh37.p13 chr5: 89,770,768-89,882,618 , GRCh38.p12 chr5: 90,474,951-90,586,801	LYSMD3, MBLAC2, 2 more genes
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
nsv906404	copy number variation	21	nstd71	human		NCBI36 chr16: 32,469,358-32,481,352 , GRCh37.p13 chr16: 32,561,857-32,573,851 , GRCh38.p12 chr16: 32,550,536-32,562,530	0
nsv908099	copy number variation	23	nstd71	human		NCBI36 chr17: 31,460,645-31,889,664 , GRCh37.p13 chr17\|NW_003315949.1: 68,401-344,487 , GRCh37.p13 chr17: 34,436,532-34,815,551 , GRCh38.p12 chr17\|NT_187614.1: 344,060-694,641	LOC102723414, TBC1D3I, 18 more genes

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