fsd1l[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
nsv3902932	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 108,207,197-108,300,186 , GRCh38.p12 chr9: 105,444,916-105,537,905	FSD1L, RALGAPA1P1
nsv3881190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 108,308,639-108,382,342 , GRCh38 chr9: 105,546,358-105,620,061	FSD1L, FKTN-AS1, 1 more genes
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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, 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	FSD1L, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	FSD1L, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	FSD1L, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	FSD1L, TDRD7, 2170 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 41

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Number of Variants: 20

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Supplemental Content

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Search details

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