MS13373 AND nstd71 - dbVar - NCBI

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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
nsv886475	copy number variation	6	nstd71	human		NCBI36 chr6: 103,007,816-103,106,000 , GRCh37.p13 chr6: 102,901,123-102,999,307 , GRCh38.p12 chr6: 102,453,248-102,551,432	TARDBPP5
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
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
nsv879229	copy number variation	1	nstd71	human		NCBI36 chr4: 68,997,831-69,085,989 , GRCh37.p13 chr4: 69,315,236-69,403,394 , GRCh38.p12 chr4: 68,449,518-68,537,676	UGT2B17, TMPRSS11E, 1 more genes
nsv906853	copy number variation	7	nstd71	human		NCBI36 chr16: 68,698,988-68,811,479 , GRCh37.p13 chr16: 70,141,487-70,253,978 , GRCh38.p12 chr16: 70,107,584-70,220,075	CLEC18C, PDPR, 3 more genes
nsv883716	copy number variation	23	nstd71	human		NCBI36 chr6: 29,969,546-29,981,029 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,167,227 , GRCh37.p13 chr6: 29,861,567-29,873,050 , GRCh38.p12 chr6: 29,893,790-29,905,273 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,161,607	HLA-A, DDX39BP1, 1 more genes
nsv893192	copy number variation	25	nstd71	human		NCBI36 chr9: 43,520,820-44,683,090 , GRCh37.p13 chr9: 43,580,824-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	GXYLT1P5, CYP4F60P, 30 more genes
nsv884758	copy number variation	27	nstd71	human		NCBI36 chr6: 32,549,254-32,563,460 , GRCh37.p13 chr6: 32,441,276-32,455,482 , GRCh38.p12 chr6: 32,473,499-32,487,705	0

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