tnxb[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
nsv4684059	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 32,020,447-32,020,770 , GRCh38.p12 chr6: 32,052,670-32,052,993	TNXB
nsv6137834	copy number variation	3	nstd102	human	not provided, Uncertain significance	GRCh37 chr6: 32,064,182-32,064,367 , GRCh38 chr6: 32,096,405-32,096,590	TNXB
nsv4578620	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,011,214-32,011,333 , GRCh38.p12 chr6: 32,043,437-32,043,556	TNXB
nsv7093354	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,064,785-32,064,877 , GRCh38 chr6: 32,097,008-32,097,100	TNXB
nsv7137005	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 32,007,026-32,008,182 , GRCh38.p12 chr6: 32,039,249-32,040,405	TNXB, CYP21A2
nsv4578646	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,009,126-32,012,493 , GRCh38.p12 chr6: 32,041,349-32,044,716	TNXB, CYP21A2
nsv3911883	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 32,051,369-32,091,833 , GRCh37 chr6: 32,019,146-32,059,610 , NCBI36 chr6: 32,127,124-32,167,588	TNXB, RNA5SP206
nsv7093367	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,006,200-32,011,669 , GRCh38.p12 chr6: 32,038,423-32,043,892	TNXB, CYP21A2
nsv4578628	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,009,126-32,011,669 , GRCh38.p12 chr6: 32,041,349-32,043,892	TNXB, CYP21A2
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	TNXB, 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	TNXB, 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	TNXB, 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	TNXB, 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	TNXB, 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	TNXB, TRR-ACG1-2, 1385 more genes
nsv4675941	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055	TNXB, AGER, 217 more genes
nsv3918916	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 32,056,178-32,117,261 , GRCh37 chr6: 31,948,199-32,009,282 , GRCh38 chr6: 31,980,422-32,041,505	TNXB, C4A, 6 more genes
nsv3915704	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 32,071,845-32,117,239 , GRCh37 chr6: 31,963,866-32,009,260 , GRCh38 chr6: 31,996,089-32,041,483	TNXB, C4A, 5 more genes
nsv3883993	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 31,969,589-32,007,227 , GRCh38.p12 chr6: 32,001,812-32,039,450	TNXB, C4A, 5 more genes
nsv3916660	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 32,056,109-32,116,990 , GRCh37 chr6: 31,948,130-32,009,011 , GRCh38 chr6: 31,980,353-32,041,234	TNXB, CYP21A2, 6 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 29

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Number of Variants: 20

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