cel[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
nsv6137681	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 135,947,000-135,947,065 , GRCh38 chr9: 133,071,613-133,071,678	CEL
nsv6112698	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 135,946,856-135,946,921 , GRCh38 chr9: 133,071,469-133,071,534	CEL
nsv3893019	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,939,032-135,955,672 , GRCh38.p12 chr9: 133,063,645-133,080,285	CEL
nsv3902637	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,940,490-135,948,528 , GRCh38.p12 chr9: 133,065,103-133,073,141	CEL
nsv6636077	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr9: 133,060,489-133,080,495 , GRCh37.p13 chr9: 135,935,876-135,955,882	CEL
nsv3893923	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,936,837-135,968,086 , GRCh38.p12 chr9: 133,061,450-133,092,699	CEL, CELP
nsv3901653	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,940,490-135,962,360 , GRCh38.p12 chr9: 133,065,103-133,086,973	CEL, CELP
nsv3905098	copy number variation	1	nstd102	human	Benign/Likely benign	GRCh37 chr9: 135,940,490-135,962,157 , GRCh38.p12 chr9: 133,065,103-133,086,770	CEL, CELP
nsv3903437	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,947,165-135,968,086 , GRCh38.p12 chr9: 133,071,778-133,092,699	CEL, CELP
nsv3907735	copy number variation	1	nstd102	human	Benign/Likely benign	GRCh37 chr9: 135,947,140-135,962,157 , GRCh38.p12 chr9: 133,071,753-133,086,770	CEL, CELP
nsv3891773	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,943,509-135,957,452 , GRCh38.p12 chr9: 133,068,122-133,082,065	CEL, CELP
nsv6636049	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr9: 133,061,658-133,086,400 , GRCh37.p13 chr9: 135,937,045-135,961,787	CEL, CELP
nsv6635987	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr9: 133,061,291-133,085,367 , GRCh37.p13 chr9: 135,936,678-135,960,754	CEL, CELP
nsv3907637	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,947,165-135,972,407 , GRCh38.p12 chr9: 133,071,778-133,097,020	CEL, RALGDS, 1 more genes
nsv3906138	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 135,947,165-135,971,724 , GRCh38.p12 chr9: 133,071,778-133,096,337	CEL, CELP, 1 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	CEL, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	CEL, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	CEL, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	CEL, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	CEL, RPL19P15, 2176 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 60

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Number of Variants: 20

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