ccn1[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
nsv4436747	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 101,953,182-102,026,137 , GRCh38.p12 chr4: 101,032,025-101,104,980	PPP3CA
nsv3873556	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 101,960,259-101,965,295 , GRCh38.p12 chr4: 101,039,102-101,044,138	PPP3CA
nsv3882261	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 101,959,144-101,960,878 , GRCh38.p12 chr4: 101,037,987-101,039,721	PPP3CA
nsv6311816	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 101,947,022-102,030,255 , GRCh38.p12 chr4: 101,025,865-101,109,098	PPP3CA
nsv6311707	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 122,722,580-122,738,011 , GRCh38.p12 chr4: 121,801,425-121,816,856	EXOSC9, CCNA2
nsv6311708	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 122,734,369-122,738,011 , GRCh38.p12 chr4: 121,813,214-121,816,856	CCNA2, EXOSC9
nsv6315092	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr4: 121,822,648-121,822,648 , GRCh37 chr4: 122,743,803-122,743,803	CCNA2, BBS7
nsv3917126	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052	SETD7, HSPD1P5, 294 more genes
nsv3901546	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611	CCN1, ROR1, 333 more genes
nsv6313574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400	CCN1, RNA5SP51, 315 more genes
nsv3886551	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986	CCN1, RNU6-1102P, 291 more genes
nsv6290265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113	LOC105379404, IL21-AS1, 218 more genes
nsv3885743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534	CCN1, ZNHIT6, 257 more genes
nsv4454000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657	CCN1, NEXN, 209 more genes
nsv3922957	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 118,273,037-134,486,822 , GRCh38 chr4: 117,351,881-133,565,667 , NCBI36 chr4: 118,492,485-134,706,272	LOC102724158, LOC105377411, 168 more genes
nsv5381774	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967	LOC112268469, LOC105377393, 159 more genes
nsv3879381	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 116,307,857-129,302,960 , GRCh38.p12 chr4: 115,386,701-128,381,805	SAR1AP3, LOC105377393, 153 more genes
nsv6313750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824	LOC105377395, SEPTIN7P14, 152 more genes
nsv3905989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 76,884,987-89,094,147 , NCBI36 chr1: 76,657,575-88,866,735 , GRCh38 chr1: 76,419,302-88,628,464	CCN1, DNAJB4, 146 more genes
nsv3885328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651	TRMT10A, TBCAP3, 86 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 60

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Number of Variants: 20

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Supplemental Content

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