IS40057 AND nstd71 - 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
nsv891485	copy number variation	111	nstd71	human		NCBI36 chr8: 137,747,933-137,932,941 , GRCh37.p13 chr8: 137,678,751-137,863,759 , GRCh38.p12 chr8: 136,666,508-136,851,516	LINC02055
nsv897250	copy number variation	18	nstd71	human		NCBI36 chr11: 38,205,782-38,296,860 , GRCh37.p13 chr11: 38,249,206-38,340,284 , GRCh38.p12 chr11: 38,227,656-38,318,734	LOC105376634
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv879440	copy number variation	8	nstd71	human		NCBI36 chr4: 70,310,066-70,428,712 , GRCh37.p13 chr4: 70,275,477-70,394,123 , GRCh38.p12 chr4: 69,409,759-69,528,405	UGT2B24P, UGT2B4, 1 more genes
nsv913871	copy number variation	1	nstd71	human		NCBI36 chr21: 43,682,962-43,699,130 , GRCh37.p13 chr21: 44,858,534-44,874,702 , GRCh38.p12 chr21: 43,438,654-43,454,822	HSF2BP, LINC00319, 1 more genes
nsv874027	copy number variation	19	nstd71	human		NCBI36 chr2: 49,715,638-49,809,930 , GRCh37.p13 chr2: 49,862,134-49,956,426 , GRCh38.p12 chr2: 49,634,996-49,729,288	0
nsv886057	copy number variation	200	nstd71	human		NCBI36 chr6: 67,065,007-67,111,682 , GRCh37.p13 chr6: 67,008,286-67,054,961 , GRCh38.p12 chr6: 66,298,393-66,345,068	0
nsv903307	copy number variation	25	nstd71	human		NCBI36 chr15: 19,788,495-19,993,878 , GRCh37.p13 chr15: 22,287,131-22,492,514 , GRCh38.p12 chr15: 21,999,180-22,204,563	, IGHV1OR15-1, 13 more genes

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