SP52571 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
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
nsv908426	copy number variation	77	nstd71	human		NCBI36 chr17: 41,785,962-41,943,845 , GRCh37.p13 chr17: 44,430,206-44,588,529 , GRCh38.p12 chr17: 46,352,840-46,511,163	LRRC37A2, ARL17A, 2 more genes
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
nsv904023	copy number variation	257	nstd71	human		NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691	LOC100422491, GOLGA8B, 5 more genes
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv909612	copy number variation	1	nstd71	human		NCBI36 chr18: 42,814,873-42,935,483 , GRCh37.p13 chr18: 44,560,875-44,681,485 , GRCh38.p12 chr18: 47,034,504-47,155,114	IER3IP1, ELOA2, 4 more genes
nsv912963	copy number variation	1	nstd71	human		NCBI36 chr20: 56,699,540-57,012,009 , GRCh37.p13 chr20: 57,266,134-57,578,614 , GRCh38.p12 chr20: 58,691,078-59,003,559	LOC107985382, LOC101927932, 11 more genes
nsv890285	copy number variation	9	nstd71	human		NCBI36 chr8: 7,683,445-7,840,086 , GRCh37.p13 chr8: 7,646,035-7,802,676 , GRCh38.p12 chr8: 7,788,513-7,945,154 , GRCh38.p12 chr8\|NW_018654717.1: 5,385,730-5,513,617	DEFB104B, DEFB106B, 18 more genes
nsv884815	copy number variation	2	nstd71	human		NCBI36 chr6: 32,560,168-32,586,132 , GRCh37.p13 chr6: 32,452,190-32,478,154 , GRCh38.p12 chr6: 32,484,413-32,510,377	0

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