fam174b[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
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	FAM174B, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	FAM174B, RNU6-18P, 1442 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	FAM174B, CHD2, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	FAM174B, TTLL13, 264 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	FAM174B, RPL31P55, 201 more genes
nsv3899918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654	FAM174B, SNRPCP18, 148 more genes
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	FAM174B, LOC105371009, 149 more genes
nsv6290316	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617	FAM174B, LOC105370964, 130 more genes
nsv3902841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 88,295,992-94,215,607 , GRCh38.p12 chr15: 87,752,761-93,672,378	FAM174B, BLM, 129 more genes
nsv6291795	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262	FAM174B, LINC00930, 106 more genes
nsv4456778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785	FAM174B, H2AZ2P1, 44 more genes
nsv3910807	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 92,170,113-93,438,995 , NCBI36 chr15: 90,514,347-91,783,228 , GRCh37 chr15: 92,713,343-93,982,224	FAM174B, H2AZ2P1, 23 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	FAM174B, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	FAM174B, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	FAM174B, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	FAM174B, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	FAM174B, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	FAM174B, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	FAM174B, CILP, 1176 more genes
nsv3917589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724	FAM174B, GAPDHP61, 840 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 60

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 60

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity