SAMN00006356 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
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
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
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
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
esv2676537	copy number variation	2	estd199	human	GRCh37 chr18: 69,428,112-69,441,441 , GRCh38.p12 chr18: 71,760,876-71,774,205	LINC01899
esv2663811	copy number variation	483	estd199	human	GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
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
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
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
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
esv2673707	copy number variation	73	estd199	human	GRCh37 chr7: 115,931,640-115,941,248 , GRCh38.p12 chr7: 116,291,586-116,301,194	LOC105375463

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 1568

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Number of Variants: 20

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