scaper[All Fields] AND 1[has_clinical] - 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
nsv6636063	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 76,884,596-76,896,941 , GRCh38.p12 chr15: 76,592,255-76,604,600	SCAPER
nsv6638085	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr15: 76,431,158-76,431,158 , GRCh37 chr15: 76,723,499-76,723,499	SCAPER
nsv3892780	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr15: 76,760,890-77,001,845 , GRCh38.p12 chr15: 76,468,549-76,709,504	SCAPER, MIR3713
nsv4675235	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr15: 77,001,844-77,112,956 , GRCh38.p12 chr15: 76,709,503-76,820,615	SCAPER, RN7SKP217
nsv6637890	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 76,842,952-77,016,134 , GRCh38.p12 chr15: 76,550,611-76,723,793	SCAPER, MIR3713
nsv4729136	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 76,617,379-76,993,135 , GRCh38.p12 chr15: 76,325,038-76,700,794	SCAPER, ISL2, 2 more genes
nsv4456590	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 76,798,898-77,110,524 , GRCh38.p12 chr15: 76,506,557-76,818,183	SCAPER, RN7SKP217, 1 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	SCAPER, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	SCAPER, RNU6-18P, 1442 more genes
nsv3913942	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 70,025,300-78,705,993 , NCBI36 chr15: 68,104,693-76,785,390 , GRCh37 chr15: 70,317,639-78,998,335	SCAPER, SNX33, 209 more genes
nsv3913830	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 76,006,154-79,982,417 , NCBI36 chr15: 74,085,550-78,061,814 , GRCh37 chr15: 76,298,495-80,274,759	SCAPER, TSPAN3, 86 more genes
nsv6637477	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055	SCAPER, PTPN9, 96 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	SCAPER, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	SCAPER, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	SCAPER, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	SCAPER, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	SCAPER, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	SCAPER, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	SCAPER, CILP, 1176 more genes
nsv3917589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724	SCAPER, GAPDHP61, 840 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 37

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Number of Variants: 20

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