slc45a2[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
nsv7097274	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 33,951,639-33,951,802 , GRCh38.p12 chr5\|NT_187551.1: 152,856-153,019 , GRCh38.p12 chr5: 33,951,534-33,951,697	SLC45A2
nsv6311761	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 33,961,548-33,964,014 , GRCh38.p12 chr5: 33,961,443-33,963,909 , GRCh38.p12 chr5\|NT_187551.1: 162,765-164,558	SLC45A2
nsv6312195	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 33,944,753-33,944,997 , GRCh38.p12 chr5\|NT_187551.1: 145,970-146,214 , GRCh38.p12 chr5: 33,944,648-33,944,892	SLC45A2
nsv6312100	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 33,982,368-33,991,527 , GRCh38.p12 chr5: 33,982,263-33,991,422	SLC45A2, AMACR, 1 more genes
nsv7093341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 33,985,092-33,985,179 , GRCh38 chr5: 33,984,987-33,985,074	SLC45A2, C1QTNF3-AMACR, 1 more genes
nsv6312291	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 33,944,753-34,008,124 , GRCh38.p12 chr5: 33,944,648-34,008,019	SLC45A2, C1QTNF3-AMACR, 2 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	SLC45A2, MEGF10, 2080 more genes
nsv3914649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397	SLC45A2, LOC105374666, 399 more genes
nsv3887142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091	SLC45A2, H3Y1, 381 more genes
nsv3910712	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394	SLC45A2, ROPN1L, 378 more genes
nsv3914100	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 30,184,899-35,249,537 , GRCh38 chr5: 30,149,035-35,213,678 , GRCh37 chr5: 30,149,142-35,213,780	SLC45A2, GUSBP18, 61 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	SLC45A2, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	SLC45A2, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	SLC45A2, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	SLC45A2, LINC02241, 878 more genes
nsv3923992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984	SLC45A2, LOC100130748, 533 more genes
nsv3911295	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 54,954-45,649,963 , NCBI36 chr5: 107,954-45,685,720 , GRCh38 chr5: 54,839-45,649,861	SLC45A2, PMCHL1, 532 more genes
nsv3922539	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 107,954-35,716,704 , GRCh37 chr5: 54,954-35,680,947 , GRCh38 chr5: 54,839-35,680,845	SLC45A2, MTCYBP37, 398 more genes
nsv3889403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-35,739,404 , GRCh38.p12 chr5: 113,461-35,739,302	SLC45A2, LOC101929003, 397 more genes
nsv3888348	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-34,041,255 , GRCh38.p12 chr5: 22,149-34,041,150	SLC45A2, RNA5SP180, 381 more genes

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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 39

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Number of Variants: 20

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Supplemental Content

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Search details

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