SP52704 AND nstd71 - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv897013	copy number variation	1	nstd71	human		NCBI36 chr11: 16,163,234-16,264,276 , GRCh37.p13 chr11: 16,206,658-16,307,700 , GRCh38.p12 chr11: 16,185,112-16,286,154	SOX6
nsv901814	copy number variation	288	nstd71	human		NCBI36 chr14: 43,558,217-43,606,201 , GRCh37.p13 chr14: 44,488,467-44,536,451 , GRCh38.p12 chr14: 44,019,264-44,067,248	LINC02307
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
nsv872736	copy number variation	1	nstd71	human		NCBI36 chr1: 188,030,954-188,041,024 , GRCh37.p13 chr1: 189,764,331-189,774,401 , GRCh38.p12 chr1: 189,795,201-189,805,271	LINC01701
nsv908425	copy number variation	235	nstd71	human		NCBI36 chr17: 41,785,962-41,922,658 , GRCh37.p13 chr17: 44,430,206-44,566,775 , GRCh38.p12 chr17: 46,352,840-46,489,976	NSFP1, ARL17B
nsv877083	copy number variation	1	nstd71	human		NCBI36 chr3: 84,803,672-84,901,837 , GRCh37.p13 chr3: 84,720,982-84,819,147 , GRCh38.p12 chr3: 84,671,831-84,769,996	TMEM183AP5, LINC00971
nsv893222	copy number variation	50	nstd71	human		NCBI36 chr9: 43,570,503-43,641,682 , GRCh37.p13 chr9: 43,630,507-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,183,882	SPATA31A6, CNTNAP3B
nsv901513	copy number variation	3	nstd71	human		NCBI36 chr14: 24,736,471-24,937,588 , GRCh37.p13 chr14: 25,666,631-25,867,748 , GRCh38.p12 chr14: 25,197,425-25,398,542	OR7K1P, HMGN2P6, 2 more genes
nsv872235	copy number variation	1	nstd71	human		NCBI36 chr1: 144,323,866-144,500,467 , GRCh37.p13 chr1\|NW_003871055.3: 2,461,342-2,638,017 , GRCh37.p13 chr1: 145,612,509-145,789,110 , GRCh38.p12 chr1: 145,645,929-145,822,604	POLR3C, CD160, 3 more genes
nsv899666	copy number variation	72	nstd71	human		NCBI36 chr12: 130,362,098-130,395,261 , GRCh37.p13 chr12: 131,796,145-131,829,308 , GRCh38.p12 chr12: 131,311,600-131,344,763	0
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv896955	copy number variation	127	nstd71	human		NCBI36 chr11: 5,828,407-5,911,385 , GRCh37.p13 chr11: 5,871,831-5,954,809 , GRCh38.p12 chr11: 5,850,601-5,933,579	OR52E7P, OR52E4, 4 more genes

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