camsap1[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
nsv3896900	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 138,798,495-138,803,846 , GRCh38.p12 chr9: 135,906,649-135,912,000	CAMSAP1, CAMSAP1-DT
nsv3897587	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 138,797,296-138,800,014 , GRCh38.p12 chr9: 135,905,450-135,908,168	CAMSAP1, CAMSAP1-DT
nsv3904101	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 138,797,296-138,799,960 , GRCh38.p12 chr9: 135,905,450-135,908,114	CAMSAP1, CAMSAP1-DT
nsv3895043	copy number variation	2	nstd102	human	Benign	GRCh37 chr9: 138,798,659-138,800,068 , GRCh38.p12 chr9: 135,906,813-135,908,222	CAMSAP1, CAMSAP1-DT
nsv3906600	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 138,798,659-138,799,960 , GRCh38.p12 chr9: 135,906,813-135,908,114	CAMSAP1, CAMSAP1-DT
nsv3904029	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 138,798,659-138,800,014 , GRCh38.p12 chr9: 135,906,813-135,908,168	CAMSAP1, CAMSAP1-DT
nsv3918779	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 137,320,520-141,049,374 , NCBI36 chr9: 136,460,341-140,169,195 , GRCh38 chr9: 134,428,674-138,154,922	CAMSAP1, LRRC26, 160 more genes
nsv3891854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 137,816,459-141,114,095 , GRCh38.p12 chr9: 134,924,613-138,223,645	CAMSAP1, LCN10, 147 more genes
nsv3899903	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,209,358-141,020,389 , GRCh38.p12 chr9: 135,317,512-138,125,937	CAMSAP1, NSMF, 137 more genes
nsv3896336	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,222,049-141,018,925 , GRCh38.p12 chr9: 135,330,203-138,124,473	CAMSAP1, LINC02907, 137 more genes
nsv4685995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549	CAMSAP1, TPRN, 137 more genes
nsv7098070	copy number variation	3	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999	CAMSAP1, STPG3-AS1, 132 more genes
nsv7093414	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409	CAMSAP1, LHX3, 121 more genes
nsv6313935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937	CAMSAP1, ENTR1, 115 more genes
nsv3922926	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 137,483,683-139,628,011 , GRCh37 chr9: 138,343,862-140,508,190 , GRCh38 chr9: 135,452,016-137,613,738	CAMSAP1, SSNA1, 126 more genes
nsv4681206	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973	CAMSAP1, DPP7, 112 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	CAMSAP1, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	CAMSAP1, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	CAMSAP1, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	CAMSAP1, OR13C1P, 2183 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 65

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Number of Variants: 20

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