kank1[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
nsv3898536	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 564,373-637,031 , GRCh38.p12 chr9: 564,373-637,031	KANK1
nsv3895415	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 581,646-602,986 , GRCh38.p12 chr9: 581,646-602,986	KANK1
nsv3898220	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 641,609-647,785 , GRCh38.p12 chr9: 641,609-647,785	KANK1
nsv3899144	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 643,453-647,862 , GRCh38.p12 chr9: 643,453-647,862	KANK1
nsv4456150	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 516,412-548,426 , GRCh38.p12 chr9: 516,412-548,426	KANK1
nsv4456331	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 661,094-689,472 , GRCh38.p12 chr9: 661,094-689,472	KANK1
nsv3895218	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 512,066-539,674 , GRCh38.p12 chr9: 512,066-539,674	KANK1
nsv6313289	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 676,973-677,029 , GRCh38.p12 chr9: 676,973-677,029	KANK1
nsv3904055	copy number variation	2	nstd102	human	Uncertain significance, Likely benign	GRCh37 chr9: 611,150-694,567 , GRCh38.p12 chr9: 611,150-694,567	KANK1, EIF1P1
nsv3911390	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr9: 582,076-684,567 , GRCh37 chr9: 592,076-694,567 , GRCh38 chr9: 592,076-694,567	KANK1, EIF1P1
nsv3908061	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 608,595-694,567 , GRCh38.p12 chr9: 608,595-694,567	KANK1, EIF1P1
nsv4457232	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 608,645-694,567 , GRCh38.p12 chr9: 608,645-694,567	KANK1, EIF1P1
nsv3894723	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr9: 608,682-694,567 , GRCh38.p12 chr9: 608,682-694,567	KANK1, EIF1P1
nsv3891449	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 608,702-694,567 , GRCh38.p12 chr9: 608,702-694,567	KANK1, EIF1P1
nsv4435995	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 611,517-690,998 , GRCh38.p12 chr9: 611,517-690,998	KANK1, EIF1P1
nsv4456059	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 512,066-579,753 , GRCh38.p12 chr9: 512,066-579,753	KANK1, RNU6-1327P
nsv3904534	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 507,002-568,398 , GRCh38.p12 chr9: 507,002-568,398	KANK1, RNU6-1327P
nsv3908853	copy number variation	1	nstd102	human	conflicting data from submitters	GRCh37 chr9: 635,338-685,819 , GRCh38.p12 chr9: 635,338-685,819	KANK1, EIF1P1
nsv3894928	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 637,962-678,832 , GRCh38.p12 chr9: 637,962-678,832	KANK1, EIF1P1
nsv6636098	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 707,446-708,017 , GRCh38 chr9: 707,446-708,017	KANK1, LOC107987042

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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 328

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Number of Variants: 20

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