SAMN00006496 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
esv2665324	copy number variation	2	estd199	human	GRCh37 chr8: 16,455,091-16,531,025 , GRCh38.p12 chr8: 16,597,582-16,673,516	LOC101929028
esv2676068	copy number variation	152	estd199	human	GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015	HLA-DRB5
esv2664200	copy number variation	92	estd199	human	GRCh37 chr4: 75,282,645-75,323,192 , GRCh38.p12 chr4: 74,416,928-74,457,475	AREG
esv2660522	copy number variation	236	estd199	human	GRCh37 chr1: 207,700,012-207,737,123 , GRCh38.p12 chr1: 207,526,667-207,563,778	CR1
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
esv2666578	copy number variation	167	estd199	human	GRCh37 chr17: 77,462,245-77,494,392 , GRCh38.p12 chr17: 79,466,163-79,498,310	RBFOX3
esv2676981	copy number variation	78	estd199	human	GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922	CYP2A6
esv2661219	copy number variation	458	estd199	human	GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103	SPIDR
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
esv2671077	copy number variation	44	estd199	human	GRCh37 chr2: 180,065,450-180,081,661 , GRCh38.p12 chr2: 179,200,723-179,216,934	SESTD1
esv2676497	copy number variation	51	estd199	human	GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253	STPG2
esv2663734	copy number variation	40	estd199	human	GRCh37 chr7: 5,936,562-5,951,173 , GRCh38.p12 chr7: 5,896,931-5,911,542	CCZ1
esv2662537	copy number variation	71	estd199	human	GRCh37 chr3: 75,567,345-75,581,692 , GRCh38.p12 chr3: 75,518,194-75,532,541	SNRPCP10
esv2661760	copy number variation	42	estd199	human	GRCh37 chr7: 62,965,045-62,979,392 , GRCh38.p12 chr7: 63,504,667-63,519,014	PHKG1P2
esv2668407	copy number variation	98	estd199	human	GRCh37 chr11: 55,445,645-55,459,892 , GRCh38.p12 chr11: 55,678,169-55,692,416	OR4P1P
esv2663062	copy number variation	52	estd199	human	GRCh37 chr7: 155,594,945-155,608,992 , GRCh38.p12 chr7: 155,802,251-155,816,298	SHH
esv2675982	copy number variation	92	estd199	human	GRCh37 chr8: 21,624,845-21,638,692 , GRCh38.p12 chr8: 21,767,333-21,781,180	GFRA2
esv2657895	copy number variation	46	estd199	human	GRCh37 chr15: 76,883,645-76,897,492 , GRCh38.p12 chr15: 76,591,304-76,605,151	SCAPER
esv2669985	copy number variation	97	estd199	human	GRCh37 chr19: 1,852,045-1,864,992 , GRCh38.p12 chr19: 1,852,046-1,864,993	KLF16
esv2675866	copy number variation	315	estd199	human	GRCh37 chr9: 113,024,576-113,037,093 , GRCh38.p12 chr9: 110,262,296-110,274,813	LOC107987114

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dbVar

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 1230

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Number of Variants: 20

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