cbs[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
nsv3873544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 44,478,235-44,485,825 , GRCh38 chr21: 43,058,125-43,065,715	CBS
nsv5673184	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr21: 44,478,245-44,485,815 , GRCh38.p12 chr21: 43,058,135-43,065,705	CBS
nsv7096097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 44,479,024-44,485,181 , GRCh38.p12 chr21: 43,058,914-43,065,071	CBS
nsv6311069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 44,492,085-44,496,976 , GRCh38.p12 chr21: 43,071,975-43,076,866	CBS
nsv5673269	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 44,488,599-44,492,323 , GRCh38.p12 chr21: 43,068,489-43,072,213	CBS
nsv6311253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 44,479,686-44,483,266 , GRCh38.p12 chr21: 43,059,576-43,063,156	CBS
nsv6311062	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr21: 43,063,029-43,063,327 , GRCh37 chr21: 44,483,139-44,483,437	CBS
nsv4683439	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr21: 44,480,531-44,482,525 , GRCh38.p12 chr21: 43,060,421-43,062,415	CBS
nsv5673424	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr21: 44,473,450-44,485,825 , GRCh38.p12 chr21: 43,053,340-43,065,715	CBS
nsv5381796	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr21: 44,473,972-44,480,656 , GRCh38.p12 chr21: 43,053,862-43,060,546	CBS
nsv6311109	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr21: 44,476,893-44,480,676 , GRCh38.p12 chr21: 43,056,783-43,060,566	CBS
nsv4684379	insertion	1	nstd102	human	Benign	GRCh38 chr21: 43,063,073-43,063,073 , GRCh37 chr21: 44,483,183-44,483,183	CBS
nsv3923210	insertion	4	nstd102	human	Benign, Likely benign	GRCh38 chr21: 43,063,062-43,063,062 , GRCh37 chr21: 44,483,172-44,483,172	CBS
nsv3923169	insertion	1	nstd102	human	Benign	GRCh38 chr21: 43,063,063-43,063,063 , GRCh37 chr21: 44,483,173-44,483,173	CBS
nsv3915139	insertion	14	nstd102	human	Benign, Likely benign	GRCh38 chr21: 43,063,074-43,063,074 , GRCh37 chr21: 44,483,184-44,483,184	CBS
nsv3902861	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 44,477,206-44,488,974 , GRCh38.p12 chr21: 43,057,096-43,068,864	CBS
nsv3885823	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr21: 44,473,450-44,477,017 , GRCh38 chr21: 43,053,340-43,056,907	CBS
nsv6311108	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 44,472,301-44,497,040 , GRCh38.p12 chr21: 43,052,191-43,076,930	CBS
nsv4683546	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 44,473,450-44,496,976 , GRCh38.p12 chr21: 43,053,340-43,076,866	CBS
nsv4450047	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 44,473,450-44,492,323 , GRCh38 chr21: 43,053,340-43,072,213	CBS

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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 105

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Number of Variants: 20

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