SAMN00006349 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
esv2676574	copy number variation	189	estd199	human	GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780	LOC105377865
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
esv2662955	copy number variation	1	estd199	human	GRCh37 chr12: 44,223,640-44,281,893 , GRCh38.p12 chr12: 43,829,837-43,888,090	TMEM117
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
esv2660065	copy number variation	70	estd199	human	GRCh37 chr22: 17,241,545-17,278,492 , GRCh38.p12 chr22: 16,760,655-16,797,602	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
esv2666277	copy number variation	79	estd199	human	GRCh37 chr7: 141,765,351-141,794,383 , GRCh38.p12 chr7: 142,065,551-142,094,583 , GRCh38.p12 chr7\|NT_187562.1: 27,431-56,463	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
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
esv2673144	copy number variation	42	estd199	human	GRCh37 chr7: 1,271,045-1,287,392 , GRCh38.p12 chr7: 1,231,409-1,247,756	UNCX
esv2665462	copy number variation	1	estd199	human	GRCh37 chr1: 41,068,430-41,084,761 , GRCh38.p12 chr1: 40,602,758-40,619,089	RIMS3
esv2658015	copy number variation	1	estd199	human	GRCh37 chr1: 41,068,350-41,084,667 , GRCh38.p12 chr1: 40,602,678-40,618,995	RIMS3
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
esv2659146	copy number variation	109	estd199	human	GRCh37 chrX: 154,790,189-154,803,312 , GRCh38.p12 chrX: 155,560,528-155,573,651	TMLHE
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
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

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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 1732

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Number of Variants: 20

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