SP53700 AND nstd71 - 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
nsv872693	copy number variation	223	nstd71	human		NCBI36 chr1: 187,587,641-187,815,034 , GRCh37.p13 chr1: 189,321,018-189,548,411 , GRCh38.p12 chr1: 189,351,888-189,579,281	LOC105371657
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
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
nsv884562	copy number variation	7	nstd71	human		NCBI36 chr6: 32,058,245-32,067,857 , GRCh37.p13 chr6\|NT_167245.1: 3,235,847-3,245,460 , GRCh37.p13 chr6\|NT_167249.1: 3,282,976-3,292,588 , GRCh37.p13 chr6: 31,950,266-31,959,878 , GRCh38.p12 chr6: 31,982,489-31,992,101 , GRCh38.p12 chr6\|NT_167245.2: 3,230,262-3,239,875 , GRCh38.p12 chr6\|NT_167249.2: 3,283,678-3,293,290	C4B_2, C4A
nsv887655	copy number variation	4	nstd71	human		NCBI36 chr7: 13,235,440-13,282,502 , GRCh37.p13 chr7: 13,268,915-13,315,977 , GRCh38.p12 chr7: 13,229,290-13,276,352	0
nsv906491	copy number variation	48	nstd71	human		NCBI36 chr16: 32,482,392-32,511,911 , GRCh37.p13 chr16: 32,574,891-32,604,410 , GRCh38.p12 chr16: 32,563,570-32,593,089	0
nsv906404	copy number variation	21	nstd71	human		NCBI36 chr16: 32,469,358-32,481,352 , GRCh37.p13 chr16: 32,561,857-32,573,851 , GRCh38.p12 chr16: 32,550,536-32,562,530	0
nsv906158	copy number variation	9	nstd71	human		NCBI36 chr16: 32,438,272-32,445,732 , GRCh37.p13 chr16: 32,530,771-32,538,231 , GRCh38.p12 chr16: 32,519,450-32,526,910	0
nsv911475	copy number variation	1	nstd71	human		NCBI36 chr19: 23,749,777-24,337,206 , GRCh37.p13 chr19: 23,957,937-24,545,366 , GRCh38.p12 chr19: 23,775,135-24,362,564	ZNF726P1, RPSA2, 8 more genes

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