sult2a1[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
nsv3906449	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 48,357,152-48,386,357 , GRCh38.p12 chr19: 47,853,895-47,883,100	SULT2A1, TPRX2, 1 more genes
nsv3892843	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,303,876-48,402,211 , GRCh38.p12 chr19: 47,800,619-47,898,954	SULT2A1, LINC01595, 3 more genes
nsv4681242	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,305,032-48,389,514 , GRCh38.p12 chr19: 47,801,775-47,886,257	SULT2A1, CRX, 3 more genes
nsv4681403	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,321,695-48,389,514 , GRCh38.p12 chr19: 47,818,438-47,886,257	SULT2A1, LINC01595, 2 more genes
nsv3907980	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,334,930-48,402,210 , GRCh38.p12 chr19: 47,831,673-47,898,953	SULT2A1, LINC01595, 2 more genes
nsv3918097	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 53,027,887-53,097,749 , GRCh37 chr19: 48,336,075-48,405,937 , GRCh38 chr19: 47,832,818-47,902,680	SULT2A1, TPRX2, 2 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	SULT2A1, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	SULT2A1, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	SULT2A1, LENG8, 2408 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	SULT2A1, ZNF461, 735 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	SULT2A1, MIR4324, 485 more genes
nsv3924836	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402	SULT2A1, IGFL1P1, 145 more genes
nsv3918983	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 46,658,791-49,050,450 , GRCh37 chr19: 47,162,048-49,553,707 , NCBI36 chr19: 51,853,888-54,245,519	SULT2A1, LOC105372432, 121 more genes
nsv4350827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279	SULT2A1, LINC01595, 59 more genes
nsv3900160	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 46,404,248-48,488,721 , GRCh38.p12 chr19: 45,900,990-47,985,464	SULT2A1, C5AR1, 84 more genes
nsv7148162	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 47,794,370-47,886,413 , GRCh37.p13 chr19: 48,297,627-48,389,670	SULT2A1, RPL23AP80, 4 more genes
nsv7148237	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 47,257,435-47,886,413 , GRCh37.p13 chr19: 47,760,692-48,389,670	SULT2A1, KPTN, 22 more genes
nsv4685764	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460	SULT2A1, SNAR-G1, 453 more genes
nsv4457853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699	SULT2A1, DHDH, 94 more genes
nsv4676184	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,043,102-48,402,210 , GRCh38.p12 chr19: 47,539,845-47,898,953	SULT2A1, RPL23AP80, 12 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 23

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Number of Variants: 20

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Supplemental Content

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