MS22297 AND nstd71 - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv887848	copy number variation	1	nstd71	human		NCBI36 chr7: 25,966,662-26,026,264 , GRCh37.p13 chr7: 26,000,137-26,059,739 , GRCh38.p12 chr7: 25,960,517-26,020,119	LOC105375199
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
nsv893231	copy number variation	140	nstd71	human		NCBI36 chr9: 43,594,114-43,641,682 , GRCh37.p13 chr9: 43,654,118-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,160,271	CNTNAP3B
nsv890777	copy number variation	14	nstd71	human		NCBI36 chr8: 39,356,825-39,469,468 , GRCh37.p13 chr8: 39,237,668-39,350,311 , GRCh38.p12 chr8: 39,380,149-39,492,792	ADAM5, ADAM3A
nsv911820	copy number variation	15	nstd71	human		NCBI36 chr19: 47,982,103-48,107,283 , GRCh37.p13 chr19: 43,290,263-43,415,443 , GRCh38.p12 chr19: 42,786,111-42,911,291	CEACAMP6, PSG1, 3 more genes
nsv888859	copy number variation	19	nstd71	human		NCBI36 chr7: 101,921,012-102,121,342 , GRCh37.p13 chr7: 102,134,007-102,334,106 , GRCh38.p12 chr7: 102,493,560-102,693,659	RASA4DP, SPDYE2B, 7 more genes
nsv904039	copy number variation	243	nstd71	human		NCBI36 chr15: 32,506,097-32,625,184 , GRCh37.p13 chr15: 34,718,805-34,837,892 , GRCh38.p12 chr15: 34,426,604-34,545,691	DNM1P5, MIR1233-2, 4 more genes
nsv898113	copy number variation	6	nstd71	human		NCBI36 chr11: 89,232,539-89,300,869 , GRCh37.p13 chr11: 89,592,891-89,661,221 , GRCh38.p12 chr11: 89,859,723-89,928,053	TRIM51BP, MTND1P35, 5 more genes
nsv884647	copy number variation	4	nstd71	human		NCBI36 chr6: 32,076,050-32,089,979 , GRCh37.p13 chr6\|NT_167245.1: 3,253,654-3,267,584 , GRCh37.p13 chr6\|NT_167249.1: 3,300,782-3,314,711 , GRCh37.p13 chr6: 31,968,072-31,982,001 , GRCh38.p12 chr6\|NT_167249.2: 3,301,484-3,315,413 , GRCh38.p12 chr6\|NT_167245.2: 3,248,069-3,261,999 , GRCh38.p12 chr6: 32,000,295-32,014,224	C4B_2, C4B, 4 more genes
nsv886410	copy number variation	11	nstd71	human		NCBI36 chr6: 95,507,138-95,942,881 , GRCh37.p13 chr6: 95,450,417-95,836,160 , GRCh38.p12 chr6: 94,740,699-95,388,284	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
nsv889099	copy number variation	1	nstd71	human		NCBI36 chr7: 118,496,990-118,655,662 , GRCh37.p13 chr7: 118,709,754-118,868,426 , GRCh38.p12 chr7: 119,069,700-119,228,372	0
nsv887355	copy number variation	1	nstd71	human		NCBI36 chr7: 4,284,934-4,367,674 , GRCh37.p13 chr7: 4,318,408-4,401,148 , GRCh38.p12 chr7: 4,278,776-4,361,517	0

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