arid1b[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
nsv3922021	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,286,551-157,414,586 , NCBI36 chr6: 157,328,243-157,456,278 , GRCh38 chr6: 156,965,417-157,093,452	ARID1B
nsv6315354	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,341,357-157,455,697 , GRCh38.p12 chr6: 157,020,223-157,134,563	ARID1B
nsv7148168	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 157,036,218-157,111,403 , GRCh37.p13 chr6: 157,357,352-157,432,537	ARID1B
nsv6315353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,377,242-157,431,665 , GRCh38.p12 chr6: 157,056,108-157,110,531	ARID1B
nsv6112725	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,405,796-157,406,039 , GRCh38.p12 chr6: 157,084,662-157,084,905	ARID1B
nsv5673596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,405,796-157,406,039 , GRCh38.p12 chr6: 157,084,662-157,084,905	ARID1B
nsv6312565	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,519,925-157,520,061 , GRCh38.p12 chr6: 157,198,791-157,198,927	ARID1B
nsv4350321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,133,792-157,495,187 , GRCh38.p12 chr6: 156,812,658-157,174,053	ARID1B
nsv4674973	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 157,201,571-157,340,945 , GRCh38.p12 chr6: 156,880,437-157,019,811	ARID1B
nsv3905951	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 157,431,664-157,482,864 , GRCh38.p12 chr6: 157,110,530-157,161,730	ARID1B
nsv4729055	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 157,402,040-157,432,660 , GRCh38.p12 chr6: 157,080,906-157,111,526	ARID1B
nsv3922737	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 157,500,306-157,506,050 , GRCh38 chr6: 157,179,172-157,184,916	ARID1B
nsv3903244	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 157,119,943-157,519,050 , GRCh38.p12 chr6: 156,798,809-157,197,916	ARID1B
nsv7097815	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 157,488,154-157,505,589 , GRCh38.p12 chr6: 157,167,020-157,184,455	ARID1B
nsv3902617	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 157,455,905-157,468,896 , GRCh38.p12 chr6: 157,134,771-157,147,762	ARID1B
nsv7097424	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 157,192,728-157,192,806 , GRCh38.p12 chr6: 156,871,594-156,871,672	ARID1B
nsv6312564	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 157,256,580-157,256,730 , GRCh38.p12 chr6: 156,935,446-156,935,596	ARID1B
nsv7097814	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr6: 157,099,064-157,529,025 , GRCh38.p12 chr6: 156,777,930-157,207,891	ARID1B, LOC115308161, 1 more genes
nsv4457068	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,068,951-157,162,523 , GRCh38.p12 chr6: 156,747,817-156,841,389	ARID1B, LOC115308161, 1 more genes
nsv7097049	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,099,064-157,150,575 , GRCh38.p12 chr6: 156,777,930-156,829,441	ARID1B, MIR4466, 1 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 64

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Number of Variants: 20

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