SAMN00006601 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
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
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
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
esv2663816	copy number variation	25	estd199	human	GRCh37 chr3: 89,394,023-89,419,406 , GRCh38.p12 chr3: 89,344,873-89,370,256	EPHA3
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
esv2660999	copy number variation	147	estd199	human	GRCh37 chr1: 169,224,745-169,246,292 , GRCh38.p12 chr1: 169,255,507-169,277,054	NME7
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
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
esv2669960	copy number variation	208	estd199	human	GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474	FGF7P3
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
esv2670748	copy number variation	204	estd199	human	GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597	SCAPER
esv2664803	copy number variation	436	estd199	human	GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597	SCAPER
esv2675979	copy number variation	520	estd199	human	GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030	MLIP

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 788

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Number of Variants: 20

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