umad1[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
nsv3900472	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 7,724,805-7,740,914 , GRCh38.p12 chr7: 7,685,174-7,701,283	UMAD1, RPA3
nsv4729199	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 7,857,363-7,985,758 , GRCh38.p12 chr7: 7,817,732-7,946,127	UMAD1, RNU6-534P, 1 more genes
nsv3908698	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 7,725,585-7,808,253 , GRCh38.p12 chr7: 7,685,954-7,768,622	UMAD1, RPA3, 2 more genes
nsv3895485	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 7,737,048-7,779,324 , GRCh38.p12 chr7: 7,697,417-7,739,693	UMAD1, LOC100533631, 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	UMAD1, RNU6-438P, 2682 more genes
nsv3914603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 6,146,033-11,052,284 , NCBI36 chr7: 6,112,559-11,018,809 , GRCh38 chr7: 6,106,402-11,012,657	UMAD1, LOC101154643, 69 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	UMAD1, 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	UMAD1, 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	UMAD1, 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	UMAD1, 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	UMAD1, RPL23AP52, 638 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	UMAD1, 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	UMAD1, 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	UMAD1, 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	UMAD1, 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	UMAD1, LOC105375156, 365 more genes
nsv3913671	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 140,213-25,227,309 , GRCh38 chr7: 45,130-25,221,165 , GRCh37 chr7: 45,130-25,260,784	UMAD1, UNCX, 363 more genes
nsv3900684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-23,674,928 , GRCh38.p12 chr7: 43,360-23,635,309	UMAD1, LOC100127955, 345 more genes
nsv3915436	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 5,688,366-27,236,455 , GRCh37 chr7: 5,721,840-27,269,930 , GRCh38 chr7: 5,682,209-27,230,311	UMAD1, LOC101154643, 295 more genes
nsv4456827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996	UMAD1, MIR6836, 277 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 45

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Number of Variants: 20

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