bbln[All Fields] AND 1[has_clinical] - dbVar

loading data ...

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	BBLN, FNBP1, 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	BBLN, DYNC2I2, 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	BBLN, MVB12B, 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	BBLN, GOLGA2, 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	BBLN, PTRH1, 99 more genes
nsv3909918	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,933,505-131,594,414 , GRCh37.p13 chr9: 130,893,684-132,554,593 , GRCh38.p12 chr9: 128,131,405-129,792,314	BBLN, C9orf50, 65 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	BBLN, PIP5KL1, 50 more genes
nsv3914825	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,873,497-130,897,002 , GRCh37.p13 chr9: 130,833,676-131,857,181 , GRCh38.p12 chr9: 128,071,397-129,094,902	BBLN, RNU7-171P, 49 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	BBLN, COQ4, 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	BBLN, RNU7-171P, 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	BBLN, EEIG1, 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	BBLN, SWI5, 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	BBLN, 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	BBLN, 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	BBLN, 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	BBLN, OR13C1P, 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	BBLN, RPL19P15, 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	BBLN, BANCR, 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	BBLN, OR2AM1P, 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	BBLN, TDRD7, 2170 more genes

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

Send to:

Search results

Items: 1 to 20 of 43

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity