MS18799 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
nsv908486	copy number variation	37	nstd71	human		NCBI36 chr17: 41,814,370-41,922,658 , GRCh37.p13 chr17: 44,458,950-44,566,775 , GRCh38.p12 chr17\|NT_187663.1: 1,118,857-1,181,521	NSF
nsv871418	copy number variation	1	nstd71	human		NCBI36 chr1: 81,382,452-81,450,354 , GRCh37.p13 chr1: 81,609,864-81,677,766 , GRCh38.p12 chr1: 81,144,179-81,212,081	RPL10AP4, LOC105378813
nsv887481	copy number variation	1	nstd71	human		NCBI36 chr7: 7,648,101-7,745,849 , GRCh37.p13 chr7: 7,681,576-7,779,324 , GRCh38.p12 chr7: 7,641,945-7,739,693	UMAD1, LOC100533631, 1 more genes
nsv880842	copy number variation	6	nstd71	human		NCBI36 chr5: 8,755,372-8,806,733 , GRCh37.p13 chr5: 8,702,372-8,753,733 , GRCh38.p12 chr5: 8,702,260-8,753,621	0
nsv873464	copy number variation	21	nstd71	human		NCBI36 chr1: 246,590,885-246,725,435 , GRCh37.p13 chr1: 248,524,262-248,658,812 , GRCh38.p12 chr1\|NT_187518.1: 8,934-149,551 , GRCh38.p12 chr1\|NT_187646.1: 8,934-145,929 , GRCh38.p12 chr1: 248,360,960-248,495,511	OR2T4, OR2T2, 7 more genes
nsv902862	copy number variation	16	nstd71	human		NCBI36 chr15: 19,116,489-19,212,282 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15\|NT_187602.1: 1-73,876	NBEAP4, LOC105370715, 4 more genes
nsv903228	copy number variation	62	nstd71	human		NCBI36 chr15: 19,635,853-19,993,878 , GRCh37.p13 chr15: 21,371,194-22,492,514 , GRCh38.p12 chr15: 21,165,865-22,204,563	LOC642131, IGHV1OR15-4, 52 more genes
nsv901296	copy number variation	150	nstd71	human		NCBI36 chr14: 19,261,709-19,494,891 , GRCh37.p13 chr14: 20,191,869-20,425,051 , GRCh38.p12 chr14: 19,723,710-19,956,892	OR4K16P, OR4K2, 12 more genes
nsv896324	copy number variation	16	nstd71	human		NCBI36 chr10: 135,075,656-135,252,190 , GRCh37.p13 chr10: 135,225,666-135,402,200 , GRCh38.p12 chr10: 133,412,162-133,588,696	SPRN, SPRNP1, 10 more genes

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