HGDP00895 AND nstd30 - 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
nsv470385	copy number variation	1	nstd30	human		NCBI36 chr7: 110,866,148-110,987,007 , GRCh37.p13 chr7: 111,078,912-111,199,771 , GRCh38.p12 chr7: 111,438,856-111,559,715	IMMP2L
nsv470433	copy number variation	34	nstd30	human		NCBI36 chr18: 64,892,426-64,906,488 , GRCh37.p13 chr18: 66,741,446-66,755,508 , GRCh38.p12 chr18: 69,074,209-69,088,271	CCDC102B
nsv471195	copy number variation	1	nstd30	human		NCBI36 chr22: 28,433,476-28,458,380 , GRCh37.p13 chr22: 30,103,476-30,128,380 , GRCh38.p12 chr22: 29,707,487-29,732,391	ZMAT5, CABP7
nsv470455	copy number variation	6	nstd30	human		NCBI36 chr2: 40,688,789-40,912,668 , GRCh37.p13 chr2: 40,835,285-41,059,164 , GRCh38.p12 chr2: 40,608,145-40,832,024	LINC01794, LOC105374473, 3 more genes
nsv471069	copy number variation	7	nstd30	human		NCBI36 chr16: 1,744,358-1,781,034 , GRCh38.p12 chr16: 1,754,356-1,791,032 , GRCh37.p13 chr16: 1,804,357-1,841,033	IGFALS, NME3, 5 more genes
nsv471066	copy number variation	22	nstd30	human		NCBI36 chr16: 883,362-1,472,838 , GRCh37.p13 chr16: 943,361-1,532,837 , GRCh38.p12 chr16: 893,361-1,482,836	CLCN7, SSTR5, 31 more genes
nsv470793	copy number variation	4	nstd30	human		NCBI36 chr6: 825,234-848,764 , GRCh37.p13 chr6: 880,234-903,764 , GRCh38.p12 chr6: 880,234-903,756	0
nsv470934	copy number variation	36	nstd30	human		GRCh38.p12 chr10: 46,157,935-47,923,579 , NCBI36 chr10: 46,410,733-47,173,619 , GRCh37.p13 chr10: 47,006,954-47,703,613 , GRCh37.p13 chr10\|NW_003871068.1: 431,049-2,010,264	CTSLP2, GDF2, 54 more genes

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