atp8b4[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
nsv3923552	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 50,043,811-50,429,349 , NCBI36 chr15: 47,831,103-48,216,641 , GRCh38 chr15: 49,751,614-50,137,152	ATP8B4, LOC102724587, 2 more genes
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	ATP8B4, 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	ATP8B4, RNU6-18P, 1442 more genes
nsv3903255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784	ATP8B4, RN7SKP101, 234 more genes
nsv3903669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,759,773-53,252,240 , GRCh38.p12 chr15: 43,467,575-52,960,043	ATP8B4, MIR4712, 188 more genes
nsv6313917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710	ATP8B4, PYGO1, 125 more genes
nsv4769387	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853	ATP8B4, BCL2L10, 86 more genes
nsv3917643	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 47,460,844-52,494,222 , GRCh37 chr15: 47,753,041-52,786,419 , NCBI36 chr15: 45,540,333-50,573,711	ATP8B4, LOC105370819, 86 more genes
nsv4675095	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529	ATP8B4, LOC102724587, 51 more genes
nsv3906553	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 47,574,384-50,369,056 , GRCh38.p12 chr15: 47,282,187-50,076,859	ATP8B4, LOC105370811, 36 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	ATP8B4, 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	ATP8B4, 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	ATP8B4, 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	ATP8B4, 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	ATP8B4, 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	ATP8B4, 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	ATP8B4, CILP, 1176 more genes
nsv6637384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239	ATP8B4, LINC03065, 228 more genes
nsv4456196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352	ATP8B4, MIR1266, 199 more genes
nsv4455359	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199	ATP8B4, MIR4716, 112 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 31

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Number of Variants: 20

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