sec11a[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
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	SEC11A, 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	SEC11A, RNU6-18P, 1442 more genes
nsv4350274	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614	SEC11A, AKAP13, 184 more genes
nsv4729284	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 83,201,955-85,786,847 , GRCh38.p12 chr15: 82,641,775-85,243,616	SEC11A, GOLGA6L5P, 77 more genes
nsv4456148	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 84,884,801-85,724,984 , GRCh38.p12 chr15: 84,216,049-85,181,753	SEC11A, NMB, 35 more genes
nsv7137120	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 84,908,070-85,681,134 , GRCh38.p12 chr15: 84,239,318-85,137,903	SEC11A, UBE2Q2P1, 32 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	SEC11A, 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	SEC11A, 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	SEC11A, 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	SEC11A, 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	SEC11A, 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	SEC11A, 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	SEC11A, 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	SEC11A, GAPDHP61, 840 more genes
nsv3895615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 64,637,227-102,509,910 , GRCh38.p12 chr15: 64,345,028-101,969,707	SEC11A, KRT18P47, 781 more genes
nsv3899560	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 71,329,220-102,270,758 , GRCh38.p12 chr15: 71,036,881-101,730,555	SEC11A, KRT8P23, 626 more genes
nsv3915187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 70,234,344-100,278,724 , GRCh37 chr15: 72,447,290-102,461,201 , GRCh38 chr15: 72,154,949-101,920,998	SEC11A, LOC102724117, 618 more genes
nsv7148092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689	SEC11A, RPL9P8, 547 more genes
nsv3890873	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 76,061,144-102,429,112 , GRCh38.p12 chr15: 75,768,803-101,888,909	SEC11A, PSTPIP1, 502 more genes
nsv3904803	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 77,479,244-102,429,112 , GRCh38.p12 chr15: 77,186,902-101,888,909	SEC11A, ADAMTS7, 480 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

Search results

Items: 1 to 20 of 60

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Number of Variants: 20

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Supplemental Content

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