kbtbd12[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
nsv3883457	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr3: 127,814,446-127,916,946 , GRCh37 chr3: 127,533,289-127,635,789	KBTBD12, LOC107986129, 2 more genes
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	KBTBD12, QTRT2, 284 more genes
nsv6311770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203	KBTBD12, HNRNPA1P23, 278 more genes
nsv6112688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144	KBTBD12, RNU4-62P, 169 more genes
nsv6112709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157	KBTBD12, OR7E97P, 160 more genes
nsv3923961	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 126,797,420-128,946,623 , GRCh37 chr3: 126,516,263-128,665,466 , NCBI36 chr3: 127,998,953-130,148,156	KBTBD12, RUVBL1-AS1, 49 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	KBTBD12, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	KBTBD12, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	KBTBD12, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	KBTBD12, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	KBTBD12, H1-10, 846 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	KBTBD12, OR7E53P, 794 more genes
nsv3912335	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 128,809,478-134,768,195 , GRCh37 chr3: 127,326,788-133,285,505 , GRCh38 chr3: 127,607,945-133,566,661	KBTBD12, ACP3, 130 more genes
nsv7096440	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 126,707,437-127,783,900 , GRCh38.p12 chr3: 126,988,594-128,065,057	KBTBD12, LOC105374094, 23 more genes
nsv3920834	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931	KBTBD12, NCK1-DT, 271 more genes
nsv7096931	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr3: 126,707,437-130,720,194 , GRCh38.p12 chr3: 126,988,594-131,001,350	KBTBD12, JMJD4P1, 104 more genes
nsv6313888	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 127,530,506-128,170,426 , GRCh38.p12 chr3: 127,811,663-128,451,583	KBTBD12, LOC102723759, 10 more genes
nsv4454341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 127,538,025-128,174,439 , GRCh38.p12 chr3: 127,819,182-128,455,596	KBTBD12, LOC105374096, 10 more genes
nsv3910866	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 127,537,345-128,170,793 , GRCh38 chr3: 127,818,502-128,451,950 , NCBI36 chr3: 129,020,035-129,653,483	KBTBD12, LOC102723759, 10 more genes
nsv6636391	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 127,540,292-128,170,755 , GRCh38.p12 chr3: 127,821,449-128,451,912	KBTBD12, MGLL, 10 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 21

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Number of Variants: 20

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Search details

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