arl4a[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
nsv3909287	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 12,725,406-12,777,556 , GRCh38.p12 chr7: 12,685,781-12,737,931	ARL4A, LOC100505995
nsv3914357	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 12,679,436-12,832,163 , GRCh37.p13 chr7: 12,712,911-12,865,638 , GRCh38.p12 chr7: 12,673,286-12,826,013	ARL4A, LOC100505995, 1 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	ARL4A, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	ARL4A, LOC107986817, 2014 more genes
nsv3915219	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,649,696-25,800,180 , GRCh38 chr7: 10,610,069-25,760,560 , NCBI36 chr7: 10,616,221-25,766,705	ARL4A, SNORD93, 176 more genes
nsv6313854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463	ARL4A, LOC107986766, 115 more genes
nsv3913922	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 9,975,653-19,356,878 , NCBI36 chr7: 9,981,805-19,363,026 , GRCh37 chr7: 10,015,280-19,396,501	ARL4A, NPM1P13, 86 more genes
nsv3912345	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 8,962,614-17,387,487 , GRCh37.p13 chr7: 8,996,089-17,420,962 , GRCh38.p12 chr7: 8,956,459-17,381,338	ARL4A, RAD17P1, 78 more genes
nsv3923125	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 11,122,492-16,479,303 , NCBI36 chr7: 11,128,644-16,485,453 , GRCh37 chr7: 11,162,119-16,518,928	ARL4A, THRAP3P3, 43 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	ARL4A, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	ARL4A, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	ARL4A, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	ARL4A, TRGV3, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	ARL4A, RPL23AP52, 638 more genes
nsv3899194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933	ARL4A, BRWD1P3, 590 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	ARL4A, MMD2, 554 more genes
nsv3903410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 704,573-29,257,946 , GRCh38.p12 chr7: 664,936-29,218,330	ARL4A, LOC100131264, 422 more genes
nsv3922329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548	ARL4A, LOC401312, 411 more genes
nsv3916683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-26,867,253 , NCBI36 chr7: 149,268-26,833,778 , GRCh38 chr7: 54,185-26,827,634	ARL4A, ZNF12, 389 more genes
nsv3916518	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 1,737,760-27,246,914 , NCBI36 chr7: 1,704,286-27,213,439 , GRCh38 chr7: 1,698,124-27,207,295	ARL4A, LOC105375156, 365 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 41

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Number of Variants: 20

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Supplemental Content

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Search details

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