amh[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
nsv3908255	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,248,683-2,260,361 , GRCh38.p12 chr19: 2,248,684-2,260,362	AMH, SF3A2, 2 more genes
nsv3902734	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,245,444-2,251,817 , GRCh38.p12 chr19: 2,245,445-2,251,818	AMH, JSRP1, 2 more genes
nsv3902881	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,245,444-2,250,236 , GRCh38.p12 chr19: 2,245,445-2,250,237	AMH, SF3A2, 1 more genes
nsv3892603	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,248,683-2,250,528 , GRCh38.p12 chr19: 2,248,684-2,250,529	AMH, SF3A2, 2 more genes
nsv3896700	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,248,683-2,253,655 , GRCh38.p12 chr19: 2,248,684-2,253,656	AMH, MIR4321, 2 more genes
nsv3904934	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,248,683-2,252,525 , GRCh38.p12 chr19: 2,248,684-2,252,526	AMH, MIR4321, 2 more genes
nsv3900475	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 2,248,882-2,252,525 , GRCh38.p12 chr19: 2,248,883-2,252,526	AMH, MIR4321, 2 more genes
nsv3910710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 1,549,143-4,288,717 , NCBI36 chr19: 1,500,143-4,239,717 , GRCh38 chr19: 1,549,144-4,288,720	AMH, EBI3, 110 more genes
nsv3913614	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,678,561-2,257,495 , GRCh37 chr19: 1,727,561-2,306,495 , GRCh38 chr19: 1,727,562-2,306,496	AMH, JSRP1, 30 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	AMH, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	AMH, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	AMH, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	AMH, SEMA6B, 299 more genes
nsv3924102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622	AMH, POLR2E, 283 more genes
nsv4457776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345	AMH, BSG, 217 more genes
nsv3923561	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472	AMH, DAPK3, 214 more genes
nsv4676189	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677	AMH, MRPL54, 198 more genes
nsv4676346	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273	AMH, AZU1, 159 more genes
nsv3909324	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,911-3,200,875 , GRCh38.p12 chr19: 260,911-3,200,877	AMH, LOC105372234, 152 more genes
nsv3915373	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,516,574-4,059,126 , GRCh37 chr19: 1,565,574-4,108,126 , GRCh38 chr19: 1,565,575-4,108,128	AMH, LOC100419704, 104 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

Search results

Items: 1 to 20 of 38

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity