SAMN00000474 AND estd199 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
esv2667872	copy number variation	147	estd199	human	GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952	DNAH14
esv2670203	copy number variation	158	estd199	human	GRCh37 chr6: 78,967,194-79,036,475 , GRCh38.p12 chr6: 78,257,477-78,326,758	LOC105377865
esv2673642	copy number variation	50	estd199	human	GRCh37 chrX: 91,853,345-91,909,992 , GRCh38.p12 chrX: 92,598,346-92,654,993	PCDH11X
esv2673583	copy number variation	519	estd199	human	GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395	SIRPB1
esv2664197	copy number variation	34	estd199	human	GRCh37 chr11: 7,809,445-7,834,142 , GRCh38.p12 chr11: 7,787,898-7,812,595 , GRCh38.p12 chr11\|NT_187583.1: 8,766-33,463 , GRCh38.p12 chr11\|NW_011332695.1: 8,766-33,465	OR5P2
esv2657875	copy number variation	20	estd199	human	GRCh37 chr7: 6,120,895-6,145,442 , GRCh38.p12 chr7: 6,081,264-6,105,811	USP42
esv2672907	copy number variation	61	estd199	human	GRCh37 chr13: 69,244,702-69,268,757 , GRCh38.p12 chr13: 68,670,570-68,694,625	RN7SL761P
esv2665317	copy number variation	65	estd199	human	GRCh37 chr11: 7,811,173-7,833,378 , GRCh38.p12 chr11: 7,789,626-7,811,831 , GRCh38.p12 chr11\|NT_187583.1: 10,494-32,699 , GRCh38.p12 chr11\|NW_011332695.1: 10,494-32,701	OR5P2
esv2666901	copy number variation	459	estd199	human	GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779	LINC01150
esv2669475	copy number variation	624	estd199	human	GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086	RNVU1-19
esv2658667	copy number variation	23	estd199	human	GRCh37 chr10: 122,769,645-122,788,992 , GRCh38.p12 chr10: 121,010,132-121,029,479	LOC105378521
esv2669049	copy number variation	26	estd199	human	GRCh37 chr2: 203,295,345-203,313,492 , GRCh38.p12 chr2: 202,430,622-202,448,769	BMPR2
esv2672582	copy number variation	25	estd199	human	GRCh37 chr10: 122,769,701-122,787,511 , GRCh38.p12 chr10: 121,010,188-121,027,998	LOC105378521
esv2662007	copy number variation	32	estd199	human	GRCh37 chr10: 122,769,701-122,787,511 , GRCh38.p12 chr10: 121,010,188-121,027,998	LOC105378521
esv2665509	copy number variation	44	estd199	human	GRCh37 chr2: 203,295,425-203,312,915 , GRCh38.p12 chr2: 202,430,702-202,448,192	BMPR2
esv2674647	copy number variation	204	estd199	human	GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081	XKR4
esv2664362	copy number variation	25	estd199	human	GRCh37 chr8: 2,251,326-2,267,068 , GRCh38.p12 chr8\|NT_187576.1: 486,536-502,278	LOC105377783
esv2671576	copy number variation	156	estd199	human	GRCh37 chr7: 100,326,645-100,341,192 , GRCh38.p12 chr7: 100,729,022-100,743,569	ZAN
esv2664165	copy number variation	220	estd199	human	GRCh37 chr7: 100,327,572-100,340,716 , GRCh38.p12 chr7: 100,729,949-100,743,093	ZAN
esv2668652	copy number variation	25	estd199	human	GRCh37 chr1: 111,377,295-111,389,642 , GRCh38.p12 chr1: 110,834,673-110,847,020	NRBF2P3

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Result Filters

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 1357

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Number of Variants: 20

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