14-0260-004 AND nstd173 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4376820	copy number variation	1	nstd173	human		GRCh37 chr3: 41,093,451-41,147,468 , GRCh38.p12 chr3: 41,051,960-41,105,977	LOC105377045
nsv4379349	copy number variation	357	nstd173	human		GRCh37 chr20: 1,560,549-1,597,997 , GRCh38.p12 chr20: 1,579,903-1,617,351	SIRPB1
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4384457	copy number variation	635	nstd173	human		GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4373753	copy number variation	13	nstd173	human		GRCh37 chr1: 1,616,990-1,672,602 , GRCh38.p12 chr1: 1,685,551-1,741,163	LOC100129381, CDK11A, 3 more genes
nsv4370069	copy number variation	8	nstd173	human		GRCh37 chr17: 61,947,107-61,977,292 , GRCh38.p12 chr17: 63,869,747-63,899,932	CSH1, GH2, 2 more genes
nsv4369028	copy number variation	48	nstd173	human		GRCh37 chr17: 34,439,965-34,477,480 , GRCh38.p12 chr17: 36,112,572-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,669-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,493-385,008	, LOC100419980, 2 more genes
nsv4375885	copy number variation	1	nstd173	human		GRCh37 chr13: 28,486,188-28,522,031 , GRCh38.p12 chr13: 27,912,051-27,947,894	PLUT, ATP5F1EP2, 1 more genes
nsv4371902	copy number variation	41	nstd173	human		GRCh37 chr6: 67,004,973-67,048,629 , GRCh38.p12 chr6: 66,295,080-66,338,736	0
nsv4376807	copy number variation	2	nstd173	human		GRCh37 chr6: 168,336,562-168,593,509 , GRCh38.p12 chr6: 167,935,882-168,192,829	FRMD1, HGC6.3, 6 more genes
nsv4386535	copy number variation	4	nstd173	human		GRCh37 chr4: 69,366,693-69,541,894 , GRCh38.p12 chr4: 68,500,975-68,676,176	UGT2B15, UGT2B17, 4 more genes
nsv4382973	copy number variation	317	nstd173	human		GRCh37 chr5: 180,378,754-180,442,428 , GRCh38.p12 chr5: 180,951,754-181,015,428	BTNL3, LOC100128762, 4 more genes

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