MS15658 AND nstd71 - dbVar - NCBI

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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
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
nsv880247	copy number variation	1	nstd71	human		NCBI36 chr4: 150,277,429-150,379,386 , GRCh37.p13 chr4: 150,057,979-150,159,936 , GRCh38.p12 chr4: 149,136,827-149,238,784	LINC02355, LINC02430
nsv893265	copy number variation	25	nstd71	human		NCBI36 chr9: 43,609,749-43,730,292 , GRCh37.p13 chr9: 43,669,753-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,144,636	CNTNAP3B, LOC100420440
nsv881877	copy number variation	1	nstd71	human		NCBI36 chr5: 69,326,897-69,455,867 , GRCh37.p13 chr5: 69,291,141-69,420,111 , GRCh38.p12 chr5\|NT_187651.1: 243,313-349,639 , GRCh38.p12 chr5: 69,995,314-70,124,284	SMN2, NAIPP2, 4 more genes
nsv911900	copy number variation	4	nstd71	human		NCBI36 chr19: 48,039,926-48,166,539 , GRCh37.p13 chr19: 43,348,086-43,474,699 , GRCh38.p12 chr19: 42,843,934-42,970,547	PSG10P, PSG7, 3 more genes
nsv907854	copy number variation	2	nstd71	human		NCBI36 chr17: 18,971,335-19,046,968 , GRCh37.p13 chr17: 19,030,610-19,106,375 , GRCh38.p12 chr17: 19,127,297-19,203,062	KYNUP1, SNORD3A, 3 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv882057	copy number variation	1	nstd71	human		NCBI36 chr5: 70,183,438-70,451,560 , GRCh37.p13 chr5: 70,147,682-70,415,804 , GRCh38.p12 chr5: 70,851,855-71,119,977	SMN1, NAIP, 9 more genes
nsv901390	copy number variation	39	nstd71	human		NCBI36 chr14: 19,317,620-19,494,891 , GRCh37.p13 chr14: 20,247,780-20,425,051 , GRCh38.p12 chr14: 19,779,621-19,956,892	OR4K3, OR4K4P, 9 more genes

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