aopep[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
nsv5674177	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,876,901-97,879,682 , GRCh38.p12 chr9: 95,114,619-95,117,400	AOPEP, FANCC
nsv4682314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,897,618-97,897,794 , GRCh38.p12 chr9: 95,135,336-95,135,512	AOPEP, FANCC
nsv4683366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,876,901-97,877,002 , GRCh38.p12 chr9: 95,114,619-95,114,720	AOPEP, FANCC
nsv5674248	insertion	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,101,753-95,101,753 , GRCh37 chr9: 97,864,035-97,864,035	AOPEP, FANCC
nsv4682250	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,897,618-98,011,661 , GRCh38.p12 chr9: 95,135,336-95,249,379	AOPEP, FANCC, 1 more genes
nsv6313117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,863,979-97,934,439 , GRCh38.p12 chr9: 95,101,697-95,172,157	AOPEP, FANCC, 3 more genes
nsv5673831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,873,735-97,897,794 , GRCh38.p12 chr9: 95,111,453-95,135,512	AOPEP, FANCC, 1 more genes
nsv7097970	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,897,618-97,912,379 , GRCh38.p12 chr9: 95,135,336-95,150,097	AOPEP, FANCC, 1 more genes
nsv6313116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,861,619-97,869,538 , GRCh38.p12 chr9: 95,099,337-95,107,256	AOPEP, FANCC, 1 more genes
nsv7098987	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 97,873,920-97,887,367 , GRCh38.p12 chr9: 95,111,638-95,125,085	AOPEP, FANCC, 1 more genes
nsv6290545	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 97,864,133-97,873,744 , GRCh38.p12 chr9: 95,101,851-95,111,462	AOPEP, FANCC, 1 more genes
nsv6635993	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 95,111,638-95,240,648 , GRCh37 chr9: 97,873,920-98,002,930	AOPEP, FANCC, 2 more genes
nsv6313118	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 95,114,619-95,172,157 , GRCh37 chr9: 97,876,901-97,934,439	AOPEP, FANCC, 2 more genes
nsv6313966	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 97,897,613-97,973,416 , GRCh38.p12 chr9: 95,135,331-95,211,134	AOPEP, RNA5SP288, 1 more genes
nsv4450968	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 97,869,338-97,869,561 , GRCh38 chr9: 95,107,056-95,107,279	AOPEP, FANCC, 1 more genes
nsv3922551	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849	AOPEP, HEMGN, 243 more genes
nsv6315179	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300	AOPEP, SUGT1P4-STRA6LP, 255 more genes
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	AOPEP, RPS26P37, 238 more genes
nsv5381561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807	AOPEP, TBC1D2, 170 more genes
nsv3922615	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 91,596,533-97,018,746 , GRCh37 chr9: 94,358,815-99,781,028 , NCBI36 chr9: 93,398,636-98,820,849	AOPEP, LOC107987097, 137 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 66

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Number of Variants: 20

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