fam102a[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
nsv3899776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507	FNBP1, MIR12126, 136 more genes
nsv3917587	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 127,795,683-131,484,475 , GRCh38 chr9: 125,993,583-129,682,375 , GRCh37 chr9: 128,755,862-132,444,654	DYNC2I2, LOC105376273, 115 more genes
nsv3924370	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225	MVB12B, MIR4672, 97 more genes
nsv3918361	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,676,681-132,287,019 , GRCh38 chr9: 127,874,581-130,421,811 , GRCh37 chr9: 130,636,860-133,297,198	GOLGA2, CRAT, 89 more genes
nsv3903209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,390,139-132,760,275 , GRCh38.p12 chr9: 127,627,860-129,997,996	PTRH1, DOLK, 99 more genes
nsv4768372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293	LOC105379841, PTRH1, 47 more genes
nsv3897949	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,079,208-130,851,795 , GRCh38.p12 chr9: 126,316,929-128,089,516	EEIG1, RNA5SP296, 44 more genes
nsv5564479	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714	PIP5KL1, MIR3911, 50 more genes
nsv4768374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685	COQ4, GLE1, 53 more genes
nsv4450425	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr9: 130,374,663-131,329,276 , GRCh38 chr9: 127,612,384-128,566,997	RNU7-171P, MIR2861, 50 more genes
nsv6312681	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,216,807-130,953,136 , GRCh38.p12 chr9: 127,454,528-128,190,857	EEIG1, PIP5KL1, 32 more genes
nsv4683557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,577,951-131,303,459 , GRCh38.p12 chr9: 127,815,672-128,541,180	SWI5, LOC105379841, 36 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	ALOX15P2, LOC107987061, 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	TBC1D13, LOC105376186, 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	MIR219A2, CLCN3P1, 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	OR13C1P, CDC37L1, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	RPL19P15, SPATA31D5P, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	BANCR, SETX, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	OR2AM1P, RN7SL565P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 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 43

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Number of Variants: 20

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