tap1[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
nsv5381623	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,269,517-33,269,568 , GRCh38.p12 chr6: 33,301,740-33,301,791	TAPBP
nsv5673673	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,276,772-33,281,549 , GRCh38 chr6: 33,308,995-33,313,772	TAPBP, ZBTB22
nsv6312574	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr6: 32,802,911-32,808,844 , GRCh38.p12 chr6: 32,835,134-32,841,067	TAP2, PSMB8
nsv7093413	delins	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,281,499-33,281,551 , GRCh38 chr6: 33,313,722-33,313,774	TAPBP, ZBTB22
nsv7093259	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 32,811,585-32,811,705 , GRCh38 chr6: 32,843,808-32,843,928	TAP1, PSMB8, 1 more genes
nsv3923205	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 25,177,008-30,177,912 , GRCh37 chr22: 26,847,008-31,847,912 , GRCh38 chr22: 26,451,042-31,451,926	DRG1, THOC5, 138 more genes
nsv3890881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,644,625-31,051,719 , GRCh38.p12 chr22: 29,248,636-30,655,732	NEFH, LOC107985541, 57 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	TAP1, 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	TAP1, 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	TAP1, 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	TAP1, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	TAP1, HLA-DPB2, 1001 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	TAP1, TRR-ACG1-2, 1385 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	LOC100419811, MTCO2P20, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	IGKV3OR22-2, ZDHHC8, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	RNU6-495P, KIAA1656, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	FBXO7, GTSE1, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	FABP5P11, SLC2A11, 1084 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	DDTL, PPP1R26P3, 1084 more genes
nsv3890401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300	YPEL1, LINC02885, 1083 more genes

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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 40

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Number of Variants: 20

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