IS40005 AND nstd71 - dbVar - NCBI

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Items: 8

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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
nsv888044	copy number variation	45	nstd71	human		NCBI36 chr7: 53,424,435-53,570,050 , GRCh37.p13 chr7: 53,456,941-53,602,556 , GRCh38.p12 chr7: 53,389,248-53,534,863	RN7SKP218, LOC105375282
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv872015	copy number variation	50	nstd71	human		NCBI36 chr1: 103,966,748-104,107,839 , GRCh37.p13 chr1: 104,165,225-104,306,316 , GRCh38.p12 chr1: 103,622,603-103,763,694	AMY1B, AMY2A, 4 more genes
nsv887510	copy number variation	7	nstd71	human		NCBI36 chr7: 8,791,785-8,834,075 , GRCh37.p13 chr7: 8,825,260-8,867,550 , GRCh38.p12 chr7: 8,785,630-8,827,920	0
nsv895324	copy number variation	1	nstd71	human		NCBI36 chr10: 47,106,350-47,454,088 , GRCh37.p13 chr10: 47,689,666-47,934,082 , GRCh38.p12 chr10: 47,438,558-47,987,500	ANXA8, AGAP9, 16 more genes
nsv890172	copy number variation	5	nstd71	human		NCBI36 chr8: 7,242,915-7,781,955 , GRCh37.p13 chr8: 7,255,505-7,744,545 , GRCh38.p12 chr8: 7,397,983-7,887,023	SPAG11A, DEFB103A, 38 more genes
nsv901296	copy number variation	150	nstd71	human		NCBI36 chr14: 19,261,709-19,494,891 , GRCh37.p13 chr14: 20,191,869-20,425,051 , GRCh38.p12 chr14: 19,723,710-19,956,892	OR4K16P, OR4K2, 12 more genes
nsv882261	copy number variation	1	nstd71	human		NCBI36 chr5: 84,055,052-84,156,824 , GRCh37.p13 chr5: 84,019,296-84,121,068 , GRCh38.p12 chr5: 84,723,478-84,825,250	0

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