SAMN00009126 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
esv2657343	copy number variation	36	estd199	human	GRCh37 chr5: 106,019,439-106,239,812 , GRCh38.p12 chr5: 106,683,738-106,904,111	LINC01950
esv2674484	copy number variation	82	estd199	human	GRCh37 chr1: 225,133,646-225,248,670 , GRCh38.p12 chr1: 224,945,944-225,060,968	DNAH14
esv2675524	copy number variation	1	estd199	human	GRCh37 chr9: 12,008,236-12,121,382 , GRCh38.p12 chr9: 12,008,236-12,121,382	LOC105375976
esv2665446	copy number variation	21	estd199	human	GRCh37 chr14: 41,608,245-41,671,292 , GRCh38.p12 chr14: 41,139,042-41,202,089	LINC02315
esv2678472	copy number variation	114	estd199	human	GRCh37 chr14: 41,609,436-41,669,664 , GRCh38.p12 chr14: 41,140,233-41,200,461	LINC02315
esv2658503	copy number variation	100	estd199	human	GRCh37 chr6: 32,454,245-32,508,892 , GRCh38.p12 chr6: 32,486,468-32,541,115	HLA-DRB5
esv2676879	copy number variation	198	estd199	human	GRCh37 chr4: 34,779,980-34,829,038 , GRCh38.p12 chr4: 34,778,358-34,827,416 , GRCh38.p12 chr4\|NW_003315915.1: 270,687-319,745	LOC105378262
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
esv2665540	copy number variation	104	estd199	human	GRCh37 chr22: 17,240,645-17,278,192 , GRCh38.p12 chr22: 16,759,755-16,797,302	XKR3
esv2668226	copy number variation	311	estd199	human	GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849	ALG1L2
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
esv2660460	copy number variation	35	estd199	human	GRCh37 chr7: 141,765,410-141,794,442 , GRCh38.p12 chr7: 142,065,610-142,094,642 , GRCh38.p12 chr7\|NT_187562.1: 27,490-56,522	MGAM
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
esv2672625	copy number variation	22	estd199	human	GRCh37 chr1: 196,772,445-196,794,492 , GRCh38.p12 chr1: 196,803,315-196,825,362	CFHR1
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
esv2667383	copy number variation	138	estd199	human	GRCh37 chr2: 98,139,645-98,158,592 , GRCh38.p12 chr2: 97,523,182-97,542,129	ANKRD36B
esv2658567	copy number variation	29	estd199	human	GRCh37 chr10: 124,341,610-124,359,750 , GRCh38.p12 chr10: 122,582,094-122,600,234	DMBT1
esv2668161	copy number variation	3	estd199	human	GRCh37 chr1: 203,907,512-203,921,936 , GRCh38.p12 chr1: 203,938,384-203,952,808	CBX1P3
esv2663153	copy number variation	1	estd199	human	GRCh37 chr10: 100,495,009-100,509,034 , GRCh38.p12 chr10: 98,735,252-98,749,277	HPSE2

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dbVar

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Object Type

Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 1897

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Number of Variants: 20

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