mitf[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
nsv3881909	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,985,770-70,014,477 , GRCh38 chr3: 69,936,619-69,965,326	MITF
nsv7097213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,985,874-70,014,399 , GRCh38.p12 chr3: 69,936,723-69,965,248	MITF
nsv6137829	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,990,469-70,005,512 , GRCh38.p12 chr3: 69,941,318-69,956,361	MITF
nsv3886136	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 69,956,353-69,965,326 , GRCh37 chr3: 70,005,504-70,014,477	MITF
nsv7096964	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,985,874-69,990,502 , GRCh38.p12 chr3: 69,936,723-69,941,351	MITF
nsv5200354	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,985,815-69,985,964 , GRCh38.p12 chr3: 69,936,664-69,936,813	MITF
nsv7096475	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr3: 70,013,978-70,014,399 , GRCh38.p12 chr3: 69,964,827-69,965,248	MITF
nsv7096816	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 69,987,065-69,997,137 , GRCh38.p12 chr3: 69,937,914-69,947,986	MITF
nsv3887493	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,850,066-69,916,637 , GRCh38.p12 chr3: 69,800,915-69,867,486	MITF
nsv3880260	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,850,066-69,902,514 , GRCh38.p12 chr3: 69,800,915-69,853,363	MITF
nsv3881853	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,763-69,920,548 , GRCh38.p12 chr3: 69,824,612-69,871,397	MITF
nsv3884532	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,726-69,900,137 , GRCh38.p12 chr3: 69,824,575-69,850,986	MITF
nsv3876159	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,763-69,881,523 , GRCh38.p12 chr3: 69,824,612-69,832,372	MITF
nsv6634555	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 70,013,475-70,013,887 , GRCh38 chr3: 69,964,324-69,964,736	MITF
nsv3872993	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,726-69,874,108 , GRCh38.p12 chr3: 69,824,575-69,824,957	MITF
nsv3871713	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,726-69,874,018 , GRCh38.p12 chr3: 69,824,575-69,824,867	MITF
nsv3871672	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,763-69,874,023 , GRCh38.p12 chr3: 69,824,612-69,824,872	MITF
nsv3879212	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,763-69,874,018 , GRCh38.p12 chr3: 69,824,612-69,824,867	MITF
nsv3889653	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,726-69,873,971 , GRCh38.p12 chr3: 69,824,575-69,824,820	MITF
nsv3888809	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 69,873,763-69,873,971 , GRCh38.p12 chr3: 69,824,612-69,824,820	MITF

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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 39

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Number of Variants: 20

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