atad3a[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
nsv5673237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 1,516,568-1,518,002 , GRCh37 chr1: 1,451,948-1,453,382	ATAD3A
nsv4578439	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 1,451,392-1,452,792 , GRCh38.p12 chr1: 1,516,012-1,517,412	ATAD3A
nsv7136955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 1,455,998-1,458,890 , GRCh38.p12 chr1: 1,520,618-1,523,510	ATAD3A
nsv5200280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,413,926-1,453,251 , GRCh38.p12 chr1: 1,478,546-1,517,871	ATAD3A, ATAD3B
nsv3879089	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,416,438-1,455,296 , GRCh38.p12 chr1: 1,481,058-1,519,916	ATAD3A, ATAD3B
nsv5200335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,416,206-1,454,423 , GRCh38.p12 chr1: 1,480,826-1,519,043	ATAD3A, ATAD3B
nsv5200325	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,420,558-1,458,389 , GRCh38.p12 chr1: 1,485,178-1,523,009	ATAD3A, ATAD3B
nsv6112691	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,418,289-1,454,405 , GRCh38.p12 chr1: 1,482,909-1,519,025	ATAD3A, ATAD3B
nsv6137750	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr1: 1,475,764-1,518,921 , GRCh37.p13 chr1: 1,411,144-1,454,301	ATAD3A, ATAD3B
nsv3876849	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 1,417,977-1,451,373 , GRCh38.p12 chr1: 1,482,597-1,515,993	ATAD3A, ATAD3B
nsv5200301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,391,729-1,461,841 , GRCh38.p12 chr1: 1,456,349-1,526,461	ATAD3A, ATAD3B, 1 more genes
nsv3886221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 1,391,287-1,460,339 , GRCh38.p12 chr1: 1,455,907-1,524,959	ATAD3A, ATAD3B, 1 more genes
nsv3876680	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 1,403,417-1,462,949 , GRCh38.p12 chr1: 1,468,037-1,527,569	ATAD3A, ATAD3B, 1 more genes
nsv4450027	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 1,380,600-1,453,590 , GRCh38.p12 chr1: 1,445,220-1,518,210	ATAD3A, ATAD3B, 1 more genes
nsv6314994	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 1,397,489-1,453,590 , GRCh38.p12 chr1: 1,462,109-1,518,210	ATAD3A, ATAD3B, 1 more genes
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	ATAD3A, RPL9P11, 466 more genes
nsv3873030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663	ATAD3A, RN7SL451P, 376 more genes
nsv3888433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316	ATAD3A, AURKAIP1, 356 more genes
nsv4436105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061	ATAD3A, PARK7, 325 more genes
nsv3899046	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775	ATAD3A, PRKCZ-DT, 315 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

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Items: 1 to 20 of 167

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Number of Variants: 20

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