SP52448 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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv888231	copy number variation	61	nstd71	human		NCBI36 chr7: 62,366,659-62,440,767 , GRCh37.p13 chr7: 62,729,224-62,803,332 , GRCh38.p12 chr7: 63,268,846-63,342,954	ZNF733P, ARAFP3
nsv882088	copy number variation	12	nstd71	human		NCBI36 chr5: 70,232,726-70,327,006 , GRCh37.p13 chr5: 70,196,970-70,291,250 , GRCh38.p12 chr5: 70,901,143-70,995,423	SMN1, SERF1A, 3 more genes
nsv881892	copy number variation	8	nstd71	human		NCBI36 chr5: 69,359,352-69,436,209 , GRCh37.p13 chr5: 69,323,596-69,400,453 , GRCh38.p12 chr5\|NT_187651.1: 253,103-329,959 , GRCh38.p12 chr5: 70,027,769-70,104,626	SERF1B, NAIPP2, 3 more genes
nsv903906	copy number variation	1	nstd71	human		NCBI36 chr15: 30,231,215-30,297,802 , GRCh37.p13 chr15: 32,443,923-32,510,510 , GRCh38.p12 chr15: 32,151,722-32,218,309	, LOC102724078, 1 more genes
nsv877489	copy number variation	2	nstd71	human		NCBI36 chr3: 131,237,362-131,337,515 , GRCh37.p13 chr3: 129,754,672-129,854,825 , GRCh38.p12 chr3: 130,035,829-130,135,982	LINC02021, FAM86HP, 3 more genes
nsv879332	copy number variation	32	nstd71	human		NCBI36 chr4: 69,097,539-69,179,871 , GRCh37.p13 chr4: 69,414,944-69,497,276 , GRCh38.p12 chr4: 68,549,226-68,631,558	LOC100132651, LOC728807, 2 more genes
nsv903770	copy number variation	10	nstd71	human		NCBI36 chr15: 28,246,827-28,492,124 , GRCh37.p13 chr15: 30,459,535-30,704,832 , GRCh38.p12 chr15: 30,167,332-30,412,629	RN7SL196P, LOC105370751, 10 more genes
nsv903953	copy number variation	1	nstd71	human		NCBI36 chr15: 30,302,218-30,514,228 , GRCh37.p13 chr15: 32,514,926-32,726,936 , GRCh38.p12 chr15: 32,222,725-32,434,735	LOC644110, DNM1P31, 9 more genes
nsv884814	copy number variation	27	nstd71	human		NCBI36 chr6: 32,560,168-32,576,147 , GRCh37.p13 chr6: 32,452,190-32,468,169 , GRCh38.p12 chr6: 32,484,413-32,500,392	0
nsv914495	copy number variation	2	nstd71	human		NCBI36 chr22: 20,646,631-20,910,314 , GRCh37.p13 chr22: 22,316,631-22,580,314 , GRCh38.p12 chr22: 21,962,259-22,225,921	IGLV1-62, IGLV4-60, 27 more genes

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