NA18960 AND nstd20 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438014	copy number variation	27	nstd20	human		NCBI34 chr8: 534,755-588,391 , GRCh37.p13 chr8: 544,755-598,391 , GRCh38.p12 chr8: 594,755-648,391	ERICH1
nsv438117	copy number variation	2	nstd20	human		NCBI34 chr9: 136,191,747-136,197,190 , GRCh37.p13 chr9: 140,973,133-140,978,576 , GRCh38.p12 chr9: 138,078,681-138,084,124	CACNA1B
nsv437862	copy number variation	3	nstd20	human		NCBI34 chr3: 62,136,076-62,139,994 , GRCh37.p13 chr3: 62,178,738-62,182,656 , GRCh38.p12 chr3: 62,193,064-62,196,982	PTPRG
nsv438011	copy number variation	95	nstd20	human		NCBI34 chr7: 141,921,685-141,931,471 , GRCh37.p13 chr7: 142,481,301-142,486,383 , GRCh38.p12 chr7\|NT_187562.1: 776,047-785,840 , GRCh37.p13 chr7\|NW_003571040.1: 956,118-965,911	TRB, PRSS3P2, 1 more genes
nsv437894	copy number variation	301	nstd20	human		NCBI34 chr3: 163,826,348-163,943,569 , GRCh37.p13 chr3: 162,505,435-162,622,656 , GRCh38.p12 chr3: 162,787,647-162,904,868	0
nsv437952	copy number variation	2	nstd20	human		NCBI34 chr4: 189,917,097-189,929,184 , GRCh37.p13 chr4: 189,221,207-189,233,294 , GRCh38.p12 chr4: 188,300,053-188,312,140	0
nsv438223	copy number variation	2	nstd20	human		NCBI34 chr12: 82,662,983-82,669,951 , GRCh37.p13 chr12: 84,160,515-84,167,483 , GRCh38.p12 chr12: 83,766,736-83,773,704	0
nsv437919	copy number variation	22	nstd20	human		NCBI34 chr4: 63,672,955-63,678,558 , GRCh37.p13 chr4: 63,669,575-63,675,178 , GRCh38.p12 chr4: 62,803,857-62,809,460	0
nsv437945	copy number variation	16	nstd20	human		NCBI34 chr4: 162,456,693-162,462,242 , GRCh37.p13 chr4: 161,879,066-161,884,615 , GRCh38.p12 chr4: 160,957,914-160,963,463	0

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