nedd9[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
nsv3921817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998	NEDD9, RN7SKP293, 230 more genes
nsv3911792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 101,974-13,964,135 , GRCh38 chr6: 156,974-13,855,925 , GRCh37 chr6: 156,974-13,856,156	NEDD9, SIRT5, 228 more genes
nsv3872373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 5,354,402-17,950,079 , GRCh38.p12 chr6: 5,354,169-17,949,848	NEDD9, TMEM14B, 189 more genes
nsv3873362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 204,009-11,608,587 , GRCh38.p12 chr6: 204,009-11,608,354	NEDD9, LOC100506207, 193 more genes
nsv3914068	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031	NEDD9, SSR1, 145 more genes
nsv3879197	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 6,990,611-11,276,452 , GRCh38.p12 chr6: 6,990,378-11,276,219	NEDD9, LOC105374904, 68 more genes
nsv3918220	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 10,601,499-13,987,316 , NCBI36 chr6: 10,709,718-14,095,526 , GRCh37 chr6: 10,601,732-13,987,547	NEDD9, GCNT2, 58 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	NEDD9, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	NEDD9, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	NEDD9, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	NEDD9, ITPR3, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	NEDD9, TRR-ACG1-2, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	NEDD9, PRELID1P2, 785 more genes
nsv3888615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006	NEDD9, LOC107986557, 349 more genes
nsv3872568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006	NEDD9, TXNDC5, 349 more genes
nsv4456780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393	NEDD9, LOC105374960, 342 more genes
nsv3886069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-21,955,964 , GRCh38.p12 chr6: 156,974-21,955,733	NEDD9, FOXCUT, 331 more genes
nsv7093363	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769	NEDD9, LOC101928354, 321 more genes
nsv3913657	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 51,431-18,468,805 , GRCh38 chr6: 106,431-18,360,595 , GRCh37 chr6: 106,431-18,360,826	NEDD9, LOC105374904, 294 more genes
nsv3922052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414	NEDD9, ECI2-DT, 268 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 28

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Number of Variants: 20

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Supplemental Content

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