SP52320 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
nsv909373	copy number variation	1	nstd71	human		NCBI36 chr18: 10,878,930-10,918,707 , GRCh37.p13 chr18: 10,888,930-10,928,707 , GRCh38.p12 chr18: 10,888,932-10,928,709	PIEZO2
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
nsv873103	copy number variation	1	nstd71	human		NCBI36 chr1: 200,386,357-200,420,206 , GRCh37.p13 chr1: 202,119,734-202,153,583 , GRCh38.p12 chr1: 202,150,606-202,184,455	PTPN7, PTPRVP
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
nsv907807	copy number variation	6	nstd71	human		NCBI36 chr17: 18,865,850-18,991,735 , GRCh37.p13 chr17: 18,925,125-19,051,010 , GRCh38.p12 chr17: 19,021,812-19,147,697	SNORD3D, KYNUP2, 7 more genes
nsv893278	copy number variation	148	nstd71	human		NCBI36 chr9: 43,616,717-44,683,090 , GRCh37.p13 chr9: 43,676,721-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	RBM17P3, RNU6-599P, 30 more genes
nsv906417	copy number variation	125	nstd71	human		NCBI36 chr16: 32,469,358-32,511,911 , GRCh37.p13 chr16: 32,561,857-32,604,410 , GRCh38.p12 chr16: 32,550,536-32,593,089	0
nsv890215	copy number variation	3	nstd71	human		NCBI36 chr8: 7,283,824-7,840,086 , GRCh37.p13 chr8: 7,296,414-7,802,676 , GRCh38.p12 chr8: 7,438,892-7,945,154	FAM90A9, SPAG11A, 39 more genes

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