apc[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
nsv3887574	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 112,780,790-112,846,239 , GRCh37 chr5: 112,116,487-112,181,936	APC
nsv7096874	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,115,546-112,179,823 , GRCh38.p12 chr5: 112,779,849-112,844,126	APC
nsv6311739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,103,097 , GRCh38.p12 chr5: 112,707,312-112,767,400	APC
nsv7097014	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,128,133-112,179,823 , GRCh38.p12 chr5: 112,792,436-112,844,126	APC
nsv7096745	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,090,742 , GRCh38.p12 chr5: 112,707,312-112,755,045	APC
nsv4681910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,090,732 , GRCh38.p12 chr5: 112,707,312-112,755,035	APC
nsv4682734	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 112,136,966-112,179,833 , GRCh38.p12 chr5: 112,801,269-112,844,136	APC
nsv6311738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,073,585 , GRCh38.p12 chr5: 112,707,312-112,737,888	APC
nsv3871022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,072,721-112,102,113 , GRCh38 chr5: 112,737,024-112,766,416	APC
nsv5673503	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,154,657-112,179,828 , GRCh38.p12 chr5: 112,818,960-112,844,131	APC
nsv7096747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,154,653-112,179,823 , GRCh38.p12 chr5: 112,818,956-112,844,126	APC
nsv3885383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,157,593-112,179,823 , GRCh38.p12 chr5: 112,821,896-112,844,126	APC
nsv3887990	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr5: 112,815,485-112,835,175 , GRCh37 chr5: 112,151,182-112,170,872	APC
nsv6315171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,155,123-112,174,165 , GRCh38.p12 chr5: 112,819,426-112,838,468	APC
nsv3883670	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 112,827,102-112,844,132 , GRCh37.p13 chr5: 112,162,799-112,179,829	APC
nsv5381608	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr5: 112,162,795-112,179,823 , GRCh38.p12 chr5: 112,827,098-112,844,126	APC
nsv1398364	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,162,805-112,179,824 , GRCh38 chr5: 112,827,108-112,844,127	APC
nsv3888529	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 112,827,923-112,844,132 , GRCh37 chr5: 112,163,620-112,179,829	APC
nsv6312084	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,154,653-112,164,679 , GRCh38.p12 chr5: 112,818,956-112,828,982	APC
nsv7093111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,036,100-112,045,850 , GRCh38.p12 chr5: 112,700,403-112,710,153	APC

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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 199

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Number of Variants: 20

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Supplemental Content

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