yy1[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
nsv3897530	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 100,701,417-100,717,821 , GRCh38.p12 chr14: 100,235,080-100,251,484	YY1
nsv3898511	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 100,691,178-100,706,973 , GRCh38.p12 chr14: 100,224,841-100,240,636	YY1
nsv3895308	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 100,704,697-100,706,973 , GRCh38.p12 chr14: 100,238,360-100,240,636	YY1
nsv3907871	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 100,704,886-100,706,973 , GRCh38.p12 chr14: 100,238,549-100,240,636	YY1
nsv4729237	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 100,655,021-100,742,092 , GRCh38.p12 chr14: 100,188,684-100,275,755	YY1, MIR6764
nsv3914561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 95,990,744-107,287,708 , GRCh38 chr14: 95,524,407-106,879,501 , NCBI36 chr14: 95,060,497-106,358,753	YY1, MIR889, 517 more genes
nsv4684265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456	YY1, NDUFB3P4, 502 more genes
nsv3911746	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 97,938,637-106,855,263 , GRCh37 chr14: 98,404,974-107,263,478 , NCBI36 chr14: 97,474,727-106,334,523	YY1, MIR1185-2, 477 more genes
nsv3921506	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 99,831,655-106,855,263 , GRCh37 chr14: 100,297,992-107,263,478 , NCBI36 chr14: 99,367,745-106,334,523	YY1, RPL21P13, 453 more genes
nsv3902723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,661,319-107,285,437 , GRCh38.p12 chr14: 100,194,982-106,877,229	YY1, NDUFB3P4, 448 more genes
nsv6291768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186	YY1, CCDC85C, 206 more genes
nsv3920123	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,729,173-102,967,034 , GRCh38 chr14: 100,262,836-102,500,697 , NCBI36 chr14: 99,798,926-102,036,787	YY1, MIR1193, 147 more genes
nsv3924299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,260,674-101,410,904 , GRCh38 chr14: 99,794,337-100,944,567 , NCBI36 chr14: 99,330,427-100,480,657	YY1, MIR433, 48 more genes
nsv7148136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125	YY1, SNORD113-5, 99 more genes
nsv3920105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,397,006-101,488,936 , GRCh38 chr14: 99,930,669-101,022,599 , NCBI36 chr14: 99,466,759-100,558,689	YY1, SNORD113-1, 82 more genes
nsv4675243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,317,190-101,012,999 , GRCh38.p12 chr14: 99,850,853-100,546,662	YY1, RN7SKP92, 20 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	YY1, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	YY1, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	YY1, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	YY1, DHRS7, 1946 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 41

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Number of Variants: 20

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Supplemental Content

Find related data

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