structure OR formation OR architecture OR conformation OR constitution - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3899090	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 83,765,377-84,013,252 , GRCh38.p12 chr12: 83,371,598-83,619,473	LOC105369874
nsv3898818	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 128,328,611-128,544,207 , GRCh38.p12 chr10: 126,640,042-126,855,638	C10orf90
nsv3900646	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr13: 85,909,019-86,064,348 , GRCh38.p12 chr13: 85,334,884-85,490,213	LINC00351
nsv3894163	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 34,546,490-34,698,627 , GRCh38.p12 chr18: 36,966,527-37,118,664	KIAA1328
nsv3886575	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 131,145,181-131,266,601 , GRCh38.p12 chr5: 131,809,488-131,930,908	MEIKIN
nsv3903155	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr13: 29,714,684-29,828,112 , GRCh38.p12 chr13: 29,140,547-29,253,975	MTUS2
nsv3887427	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 76,848,167-76,951,689 , GRCh38.p12 chr3: 76,799,016-76,902,538	ROBO2
nsv3902243	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 40,567,422-40,660,470 , GRCh38.p12 chr11: 40,545,872-40,638,920	LRRC4C
nsv3882011	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 134,978,716-135,053,549 , GRCh38.p12 chr3: 135,259,874-135,334,707	EPHB1
nsv3896610	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 9,919,638-9,990,269 , GRCh38.p12 chr9: 9,919,638-9,990,269	PTPRD
nsv3898270	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 84,429,584-84,490,643 , GRCh38.p12 chr16: 84,395,978-84,457,037	ATP2C2
nsv3890129	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 10,447,116-10,504,819 , GRCh38.p12 chr8: 10,589,606-10,647,309 , GRCh38.p12 chr8\|NW_018654717.1: 2,699,773-2,757,432	RP1L1
nsv3889078	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 39,982,433-40,037,717 , GRCh38.p12 chr2: 39,755,293-39,810,577	THUMPD2
nsv3873989	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 85,561,190-85,612,793 , GRCh38.p12 chr3: 85,512,040-85,563,643	CADM2
nsv3908056	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 99,519,242-99,568,648 , GRCh38.p12 chr11: 99,648,511-99,697,917	CNTN5
nsv3909639	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 15,062,923-15,103,156 , GRCh38.p12 chr20: 15,082,277-15,122,510	MACROD2
nsv3904305	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr20: 4,931,970-4,972,088 , GRCh38.p12 chr20: 4,951,324-4,991,442	SLC23A2
nsv3890721	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 71,608,781-71,646,728 , GRCh38.p12 chr8: 70,696,546-70,734,493	XKR9
nsv3881452	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 133,927,604-133,963,658 , GRCh38.p12 chr2: 133,170,032-133,206,086	NCKAP5
nsv3894778	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 84,435,058-84,470,476 , GRCh38.p12 chr16: 84,401,452-84,436,870	ATP2C2

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Result Filters

Object Type

Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 1785

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Number of Variants: 20

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