abca1[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
nsv7097678	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 107,547,657-107,550,868 , GRCh38.p12 chr9: 104,785,376-104,788,587	ABCA1
nsv3900569	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 107,596,285-107,598,740 , GRCh38.p12 chr9: 104,834,004-104,836,459	ABCA1
nsv3904011	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 107,596,285-107,597,707 , GRCh38.p12 chr9: 104,834,004-104,835,426	ABCA1
nsv3907976	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 107,596,285-107,597,151 , GRCh38.p12 chr9: 104,834,004-104,834,870	ABCA1
nsv6312670	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 107,645,300-107,665,960 , GRCh38.p12 chr9: 104,883,019-104,903,679	ABCA1
nsv3891722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 104,604,851-126,253,089 , GRCh38.p12 chr9: 101,842,569-123,490,810	ABCA1, LOC107987013, 326 more genes
nsv3917989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 102,112,198-118,529,754 , NCBI36 chr9: 101,152,019-117,569,575 , GRCh38 chr9: 99,349,916-115,767,475	ABCA1, CTNNAL1, 262 more genes
nsv3922633	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312	ABCA1, RAD23B, 262 more genes
nsv3922551	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849	ABCA1, HEMGN, 243 more genes
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	ABCA1, RPS26P37, 238 more genes
nsv3910258	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 99,024,205-109,947,890 , GRCh37 chr9: 101,786,487-112,710,170 , NCBI36 chr9: 100,826,308-111,749,991	ABCA1, LOC105376191, 167 more genes
nsv3891403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 103,271,401-113,948,226 , GRCh38.p12 chr9: 100,509,119-111,185,946	ABCA1, LOC112268038, 158 more genes
nsv3916125	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 103,767,420-112,984,794 , NCBI36 chr9: 105,569,522-114,786,895 , GRCh37 chr9: 106,529,701-115,747,074	ABCA1, FRRS1L, 149 more genes
nsv3895960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 106,487,247-114,541,579 , GRCh38.p12 chr9: 103,724,965-111,779,299	ABCA1, LOC105376196, 128 more genes
nsv7148263	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320	ABCA1, ACTL7B, 88 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	ABCA1, 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	ABCA1, 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	ABCA1, 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	ABCA1, 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	ABCA1, 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 47

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Number of Variants: 20

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