tafa4[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
nsv3916461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960	TAFA4, LOC105377171, 323 more genes
nsv3922768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938	TAFA4, RNU6-557P, 147 more genes
nsv6290933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004	TAFA4, NDUFB4P1, 110 more genes
nsv3883532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 66,133,719-75,076,440 , GRCh38.p12 chr3: 66,148,044-75,027,289	TAFA4, PSMD12P1, 93 more genes
nsv3917061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 68,940,430-75,092,800 , GRCh37.p13 chr3: 68,857,740-75,010,110 , GRCh38.p12 chr3: 68,808,589-74,960,959	TAFA4, RYBP, 69 more genes
nsv3920193	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 67,441,430-73,463,152 , NCBI36 chr3: 67,524,120-73,545,842 , GRCh38 chr3: 67,391,006-73,414,001	TAFA4, RNPC3P1, 65 more genes
nsv5564432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267	TAFA4, CCDC137P1, 39 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	TAFA4, 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	TAFA4, 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	TAFA4, RPL23AP49, 2875 more genes
nsv3913280	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 68,460,820-76,896,160 , GRCh37 chr3: 68,378,130-76,813,470 , GRCh38 chr3: 68,328,980-76,764,319	TAFA4, AKR1B1P2, 105 more genes
nsv6290256	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 67,610,844-69,023,278 , GRCh38.p12 chr3: 67,560,420-68,974,127	TAFA4, COPS8P2, 9 more genes
nsv3917310	copy number variation	1	nstd102	human	conflicting data from submitters	GRCh37 chr3: 67,612,239-69,023,348 , GRCh38 chr3: 67,561,815-68,974,197 , NCBI36 chr3: 67,694,929-69,106,038	TAFA4, SUCLG2, 9 more genes
nsv3889812	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 67,612,239-69,023,348 , GRCh38.p12 chr3: 67,561,815-68,974,197	TAFA4, LOC107986019, 9 more genes
nsv3917868	copy number variation	1	nstd102	human	conflicting data from submitters	NCBI36 chr3: 67,699,951-69,091,886 , GRCh37 chr3: 67,617,261-69,009,196 , GRCh38 chr3: 67,566,837-68,960,045	TAFA4, TAFA1, 8 more genes
nsv3879956	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 67,617,261-68,950,039 , GRCh38.p12 chr3: 67,566,837-68,900,888	TAFA4, PSMC1P1, 8 more genes
nsv3919623	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 67,645,351-68,960,528 , GRCh38 chr3: 67,594,927-68,911,377 , NCBI36 chr3: 67,728,041-69,043,218	TAFA4, RPLP0P8, 8 more genes
nsv3875054	copy number variation	1	nstd102	human	not provided	GRCh37 chr3: 68,461,188-69,158,250 , GRCh38.p12 chr3: 68,412,038-69,109,099	TAFA4, RPLP0P8, 10 more genes
nsv3922389	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 67,872,509-68,965,664 , GRCh38 chr3: 67,822,085-68,916,513 , NCBI36 chr3: 67,955,199-69,048,354	TAFA4, RPLP0P8, 7 more genes
nsv6290797	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 68,968,872-70,829,637 , GRCh38.p12 chr3: 68,919,721-70,780,486	TAFA4, UBA3, 17 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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Supplemental Content

Find related data

Search details

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