dbVar for Gene (Select 57002) - 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
nsv6837319	copy number variation	1	nstd229	human		GRCh38 chr7: 39,591,655-39,592,644 , GRCh37.p13 chr7: 39,631,254-39,632,243	YAE1
nsv6834393	copy number variation	1	nstd229	human		GRCh38 chr7: 38,944,248-39,960,814 , GRCh37.p13 chr7: 38,983,848-40,000,413	LOC100422519, LOC646999, 21 more genes
nsv6832877	copy number variation	1	nstd229	human		GRCh38 chr7: 39,573,513-39,583,557 , GRCh37.p13 chr7: 39,613,112-39,623,156	YAE1
nsv6831308	copy number variation	1	nstd229	human		GRCh38 chr7: 39,586,201-39,590,900 , GRCh37.p13 chr7: 39,625,800-39,630,499	YAE1
nsv6831088	copy number variation	1	nstd229	human		GRCh38 chr7: 39,567,501-39,602,400 , GRCh37.p13 chr7: 39,607,100-39,641,999	YAE1, TMX1P1
nsv6827959	copy number variation	1	nstd229	human		GRCh38 chr7: 39,384,078-39,613,245 , GRCh37.p13 chr7: 39,423,677-39,652,844	POU6F2, LOC105375237, 6 more genes
nsv6826093	copy number variation	1	nstd229	human		GRCh38 chr7: 39,582,550-39,582,956 , GRCh37.p13 chr7: 39,622,149-39,622,555	YAE1
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	RRBP1P1, SLC29A4P1, 2680 more genes
nsv6631947	copy number variation	1	nstd224	human		GRCh37 chr7: 39,623,495-40,037,248 , GRCh38.p12 chr7: 39,583,896-39,997,649	YAE1, SSBP3P1, 12 more genes
nsv6619831	copy number variation	1	nstd223	human		GRCh38 chr7: 39,606,876-39,610,719 , GRCh37.p13 chr7: 39,646,475-39,650,318	YAE1, LOC646999
nsv6619534	copy number variation	1	nstd223	human		GRCh38 chr7: 39,559,101-39,632,800 , GRCh37.p13 chr7: 39,598,700-39,672,399	YAE1, TMX1P1, 4 more genes
nsv6618138	copy number variation	1	nstd223	human		GRCh38 chr7: 39,591,655-39,592,644 , GRCh37.p13 chr7: 39,631,254-39,632,243	YAE1
nsv6617283	copy number variation	1	nstd223	human		GRCh38 chr7: 39,599,101-39,633,700 , GRCh37.p13 chr7: 39,638,700-39,673,299	RALA, LOC646999, 2 more genes
nsv6616384	copy number variation	1	nstd223	human		GRCh38 chr7: 39,607,201-39,615,700 , GRCh37.p13 chr7: 39,646,800-39,655,299	LOC646999, YAE1
nsv6614017	copy number variation	1	nstd223	human		GRCh38 chr7: 39,593,714-39,602,946 , GRCh37.p13 chr7: 39,633,313-39,642,545	YAE1
nsv6609838	copy number variation	1	nstd223	human		GRCh38 chr7: 39,599,788-39,600,366 , GRCh37.p13 chr7: 39,639,387-39,639,965	YAE1
nsv6609418	copy number variation	1	nstd223	human		GRCh38 chr7: 39,384,078-39,613,241 , GRCh37.p13 chr7: 39,423,677-39,652,840	LOC646999, POU6F2-AS1, 6 more genes
nsv6605707	copy number variation	1	nstd223	human		GRCh38 chr7: 39,554,001-39,640,200 , GRCh37.p13 chr7: 39,593,600-39,679,799	YAE1-DT, RALA, 4 more genes
nsv6605387	copy number variation	1	nstd223	human		GRCh38 chr7: 39,586,173-39,590,869 , GRCh37.p13 chr7: 39,625,772-39,630,468	YAE1
nsv6603641	copy number variation	1	nstd223	human		GRCh38 chr7: 39,600,201-39,630,200 , GRCh37.p13 chr7: 39,639,800-39,669,799	YAE1, RALA, 2 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 245

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Number of Variants: 20

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