SAMN00001663 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
esv2674624	copy number variation	1	estd199	human	GRCh37 chr8: 50,873,384-50,964,956 , GRCh38.p12 chr8: 49,960,824-50,052,396	SNTG1
esv2666739	copy number variation	325	estd199	human	GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547	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
esv2676662	copy number variation	263	estd199	human	GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591	CYP2A7
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
esv2671157	copy number variation	55	estd199	human	GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160	LOC105377865
esv2662905	copy number variation	26	estd199	human	GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160	LOC105377865
esv2662873	copy number variation	30	estd199	human	GRCh37 chr8: 75,311,432-75,330,080 , GRCh38.p12 chr8: 74,399,197-74,417,845	GDAP1
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
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
esv2656701	copy number variation	437	estd199	human	GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001	WWOX
esv2670295	copy number variation	118	estd199	human	GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754	ZBTB20
esv2660593	copy number variation	56	estd199	human	GRCh37 chrX: 91,610,345-91,620,792 , GRCh38.p12 chrX: 92,355,346-92,365,793	PCDH11X
esv2672284	copy number variation	80	estd199	human	GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666	CWF19L2
esv2673551	copy number variation	872	estd199	human	GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616	VEZF1P1
esv2673465	copy number variation	3	estd199	human	GRCh37 chr10: 86,738,671-86,748,747 , GRCh38.p12 chr10: 84,978,915-84,988,991	LOC107984249
esv2657260	copy number variation	826	estd199	human	GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083	LINC01943
esv2675622	copy number variation	1	estd199	human	GRCh37 chr6: 149,676,765-149,685,714 , GRCh38.p12 chr6: 149,355,629-149,364,578	TAB2
esv2666144	copy number variation	73	estd199	human	GRCh37 chr17: 77,992,012-78,000,841 , GRCh38.p12 chr17: 80,018,213-80,027,042	TBC1D16

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dbVar

Result Filters

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Organism

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 1745

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Number of Variants: 20

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