slc20a2[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
nsv3893373	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 42,301,152-42,354,257 , GRCh38.p12 chr8: 42,443,634-42,496,739	SLC20A2
nsv4436690	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 42,275,320-42,302,163 , GRCh38 chr8: 42,417,802-42,444,645	SLC20A2
nsv4436313	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 42,297,172-42,317,413 , GRCh38 chr8: 42,439,654-42,459,895	SLC20A2
nsv7093517	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr8: 42,462,995-42,462,995 , GRCh37 chr8: 42,320,513-42,320,513	SLC20A2
nsv3919419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 34,169,768-43,014,044 , GRCh38 chr8: 34,312,250-43,158,901 , NCBI36 chr8: 34,289,310-43,133,201	SLC20A2, PLEKHA2, 135 more genes
nsv3922311	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 37,428,611-47,058,107 , GRCh37.p13 chr8: 37,309,453-46,938,942 , GRCh38.p12 chr8: 37,451,935-46,027,320	SLC20A2, CHRNB3, 120 more genes
nsv3897112	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 42,303,397-43,002,481 , GRCh38.p12 chr8: 42,445,879-43,147,338	SLC20A2, HOOK3, 13 more genes
nsv6637131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 42,303,398-43,002,481 , GRCh38.p12 chr8: 42,445,880-43,147,338	SLC20A2, RNU1-124P, 13 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	SLC20A2, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	SLC20A2, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	SLC20A2, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	SLC20A2, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	SLC20A2, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	SLC20A2, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	SLC20A2, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	SLC20A2, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	SLC20A2, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	SLC20A2, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	SLC20A2, LOC112268023, 2103 more genes
nsv3906425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385	SLC20A2, LOC112268016, 1819 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 57

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Number of Variants: 20

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