SAMN00006534 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
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
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
esv2668553	copy number variation	22	estd199	human	GRCh37 chr17: 6,101,838-6,126,946 , GRCh38.p12 chr17: 6,198,518-6,223,626	RNU6-1264P
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
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
esv2656841	copy number variation	8	estd199	human	GRCh37 chr7: 111,941,766-111,963,145 , GRCh38.p12 chr7: 112,301,711-112,323,090	ZNF277
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
esv2663811	copy number variation	483	estd199	human	GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
esv2672976	copy number variation	16	estd199	human	GRCh37 chr7: 48,581,294-48,592,638 , GRCh38.p12 chr7: 48,541,698-48,553,042	ABCA13
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
esv2669532	copy number variation	127	estd199	human	GRCh37 chr6: 81,283,718-81,293,577 , GRCh38.p12 chr6: 80,574,001-80,583,860	LOC112267962
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

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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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Items: 1 to 20 of 915

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Number of Variants: 20

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