slc49a4[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
nsv3921899	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 123,886,249-124,237,935 , GRCh37.p13 chr3: 122,403,559-122,755,245 , GRCh38.p12 chr3: 122,684,712-123,036,398	SLC49A4, SEMA5B, 3 more genes
nsv4673955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 122,408,684-122,753,973 , GRCh38.p12 chr3: 122,689,837-123,035,126	SLC49A4, SEMA5B, 3 more genes
nsv3878386	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 122,478,089-122,635,129 , GRCh38.p12 chr3: 122,759,242-122,916,282	SLC49A4, HSPBAP1, 2 more genes
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	SLC49A4, NECTIN3, 418 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	SLC49A4, MTCO2P29, 401 more genes
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	SLC49A4, QTRT2, 284 more genes
nsv6311770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203	SLC49A4, HNRNPA1P23, 278 more genes
nsv3919464	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 114,122,562-124,532,374 , GRCh37 chr3: 113,841,409-124,251,221 , NCBI36 chr3: 115,324,099-125,733,911	SLC49A4, B4GALT4-AS1, 144 more genes
nsv6112688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144	SLC49A4, RNU4-62P, 169 more genes
nsv3924082	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573	SLC49A4, MYLK-AS2, 165 more genes
nsv3923097	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577	SLC49A4, POGLUT1, 141 more genes
nsv3913250	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 123,126,684-127,983,782 , GRCh38 chr3: 121,925,147-126,782,249 , GRCh37 chr3: 121,643,994-126,501,092	SLC49A4, RPS24P9, 106 more genes
nsv3909926	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 121,644,209-125,676,353 , NCBI36 chr3: 122,845,746-126,877,887 , GRCh37 chr3: 121,363,056-125,395,197	SLC49A4, MIR5092, 66 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	SLC49A4, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	SLC49A4, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	SLC49A4, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	SLC49A4, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	SLC49A4, H1-10, 846 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	SLC49A4, OR7E53P, 794 more genes
nsv7096531	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800	SLC49A4, MEMO1P6, 62 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 22

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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