stoml1[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	STOML1, 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	STOML1, 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	STOML1, SNX33, 209 more genes
nsv7137210	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891	STOML1, LOC105370892, 99 more genes
nsv3895410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-76,072,324 , GRCh38.p12 chr15: 72,650,843-75,779,983	STOML1, UBL7-DT, 97 more genes
nsv3920020	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966	STOML1, STRA6, 91 more genes
nsv3914896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,963,970-75,954,617 , GRCh38 chr15: 72,671,629-75,662,276 , NCBI36 chr15: 70,751,023-73,741,672	STOML1, CYP1A1, 88 more genes
nsv6309590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,978,569-75,722,716 , GRCh38.p12 chr15: 72,686,228-75,430,375	STOML1, NPM1P42, 82 more genes
nsv3905553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-75,567,198 , GRCh38.p12 chr15: 72,650,843-75,274,857	STOML1, SEMA7A, 74 more genes
nsv4455687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183	STOML1, SCAMP2, 74 more genes
nsv3903760	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,958,539-75,569,605 , GRCh38.p12 chr15: 72,666,198-75,277,264	STOML1, LOC105370893, 73 more genes
nsv3888972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,958,539-75,569,605 , GRCh38.p12 chr15: 72,666,198-75,277,264	STOML1, NEO1, 73 more genes
nsv4455940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183	STOML1, TBC1D21, 72 more genes
nsv3914282	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 70,751,023-73,322,383 , GRCh37 chr15: 72,963,970-75,535,330 , GRCh38 chr15: 72,671,629-75,242,989	STOML1, CLK3, 69 more genes
nsv491514	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr15: 72,671,374-75,680,568 , GRCh37 chr15: 72,963,715-75,972,909	STOML1, BBS4, 91 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	STOML1, 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	STOML1, 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	STOML1, 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	STOML1, 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	STOML1, FAM81A, 1614 more genes

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Number of Variants: 20

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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 42

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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