cacng3[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
nsv3905855	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846	CACNG3, LOC107984874, 217 more genes
nsv6290289	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981	CACNG3, LOC105371149, 166 more genes
nsv3891271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,379,628-29,379,768 , GRCh38.p12 chr16: 21,368,307-29,368,447	CACNG3, LOC101927814, 159 more genes
nsv6289847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924	CACNG3, GAPDHP35, 154 more genes
nsv7137115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396	CACNG3, OTOAP1, 148 more genes
nsv3924349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,612,313-28,334,665 , GRCh38 chr16: 21,600,992-28,323,344 , NCBI36 chr16: 21,519,814-28,242,166	CACNG3, SLC5A11, 111 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	CACNG3, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	CACNG3, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	CACNG3, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	CACNG3, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	CACNG3, FTLP14, 1868 more genes
nsv4685985	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630	CACNG3, LOC105371069, 654 more genes
nsv1398297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355	CACNG3, BMERB1, 701 more genes
nsv4729901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272	CACNG3, NPIPB9, 597 more genes
nsv6637429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029	CACNG3, MIR6511B2, 535 more genes
nsv3910441	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820	CACNG3, LOC729945, 450 more genes
nsv3917409	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 14,956,252-28,225,665 , GRCh37 chr16: 15,048,751-28,318,164 , GRCh38 chr16: 14,954,894-28,306,843	CACNG3, SLC7A5P2, 251 more genes
nsv3896782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 18,238,275-30,177,240 , GRCh38.p12 chr16: 18,144,418-30,165,919	CACNG3, SMG1P4, 287 more genes
nsv3900243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 19,424,115-30,142,220 , GRCh38.p12 chr16: 19,412,793-30,130,899	CACNG3, RNU6-944P, 253 more genes
nsv6637633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919	CACNG3, USP31, 200 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 35

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Number of Variants: 20

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Supplemental Content

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Search details

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