SAMN00007839 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
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
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
esv2667297	copy number variation	10	estd199	human	GRCh37 chr1: 189,415,645-189,438,742 , GRCh38.p12 chr1: 189,446,515-189,469,612	LOC105371657
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
esv2666779	copy number variation	14	estd199	human	GRCh37 chr2: 203,295,245-203,314,492 , GRCh38.p12 chr2: 202,430,522-202,449,769	BMPR2
esv2669175	copy number variation	12	estd199	human	GRCh37 chr7: 149,863,195-149,881,292 , GRCh38.p12 chr7: 150,166,106-150,184,203	ACTR3C
esv2665509	copy number variation	44	estd199	human	GRCh37 chr2: 203,295,425-203,312,915 , GRCh38.p12 chr2: 202,430,702-202,448,192	BMPR2
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
esv2671576	copy number variation	156	estd199	human	GRCh37 chr7: 100,326,645-100,341,192 , GRCh38.p12 chr7: 100,729,022-100,743,569	ZAN
esv2663029	copy number variation	12	estd199	human	GRCh37 chr1: 111,378,345-111,388,842 , GRCh38.p12 chr1: 110,835,723-110,846,220	NRBF2P3
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
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
esv2677767	copy number variation	161	estd199	human	GRCh37 chr4: 21,369,090-21,376,907 , GRCh38.p12 chr4: 21,367,467-21,375,284	KCNIP4
esv2668452	copy number variation	609	estd199	human	GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643	LOC105378113
esv2663098	copy number variation	56	estd199	human	GRCh37 chr3: 22,279,322-22,286,417 , GRCh38.p12 chr3: 22,237,830-22,244,925	ZNF385D
esv2671123	copy number variation	287	estd199	human	GRCh37 chr4: 107,056,578-107,063,364 , GRCh38.p12 chr4: 106,135,421-106,142,207	TBCK
esv2662988	copy number variation	516	estd199	human	GRCh37 chr12: 45,903,153-45,909,939 , GRCh38.p12 chr12: 45,509,370-45,516,156	LOC105369743
esv2673118	copy number variation	530	estd199	human	GRCh37 chr6: 136,582,615-136,589,299 , GRCh38.p12 chr6: 136,261,477-136,268,161	BCLAF1
esv2656489	copy number variation	507	estd199	human	GRCh37 chr9: 15,815,306-15,821,940 , GRCh38.p12 chr9: 15,815,308-15,821,942	CCDC171

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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

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Items: 1 to 20 of 821

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Number of Variants: 20

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