dbVar for Gene (Select 6540) - 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
nsv6112763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799	GALNT8, LINC02371, 197 more genes
nsv5915826	copy number variation	1	nstd209	human		GRCh38 chr12: 248,146-251,637 , GRCh37.p13 chr12: 357,312-360,803	SLC6A13, LOC102723544
nsv5914928	copy number variation	1	nstd209	human		GRCh38 chr12: 239,093-239,248 , GRCh37.p13 chr12: 348,259-348,414	SLC6A13
nsv5911809	copy number variation	1	nstd209	human		GRCh38 chr12: 239,093-239,326 , GRCh37.p13 chr12: 348,259-348,492	SLC6A13
nsv5866903	copy number variation	1	nstd209	human		GRCh38 chr12: 252,601-255,924 , GRCh37.p13 chr12: 361,767-365,090	LOC102723544, SLC6A13
nsv5866529	copy number variation	1	nstd209	human		GRCh38 chr12: 240,907-246,900 , GRCh37.p13 chr12: 350,073-356,066	SLC6A13
nsv5865795	copy number variation	1	nstd209	human		GRCh38 chr12: 236,122-239,056 , GRCh37.p13 chr12: 345,288-348,222	SLC6A13
nsv5863731	copy number variation	1	nstd209	human		GRCh38 chr12: 220,456-223,054 , GRCh37.p13 chr12: 329,622-332,220	SLC6A13
nsv5860915	copy number variation	1	nstd209	human		GRCh38 chr12: 223,955-226,454 , GRCh37.p13 chr12: 333,121-335,620	SLC6A13
nsv5860798	copy number variation	1	nstd209	human		GRCh38 chr12: 243,357-245,756 , GRCh37.p13 chr12: 352,523-354,922	SLC6A13
nsv5859703	copy number variation	1	nstd209	human		GRCh38 chr12: 224,055-228,254 , GRCh37.p13 chr12: 333,221-337,420	SLC6A13
nsv5859042	copy number variation	1	nstd209	human		GRCh38 chr12: 232,717-236,521 , GRCh37.p13 chr12: 341,883-345,687	SLC6A13
nsv5857706	copy number variation	1	nstd209	human		GRCh38 chr12: 248,201-251,500 , GRCh37.p13 chr12: 357,367-360,666	SLC6A13, LOC102723544
nsv5857623	copy number variation	1	nstd209	human		GRCh38 chr12: 261,759-264,519 , GRCh37.p13 chr12: 370,925-373,685	SLC6A13
nsv5857161	copy number variation	1	nstd209	human		GRCh38 chr12: 215,551-218,854 , GRCh37.p13 chr12: 324,717-328,020	SLC6A13
nsv5856203	copy number variation	1	nstd209	human		GRCh38 chr12: 220,455-226,254 , GRCh37.p13 chr12: 329,621-335,420	SLC6A13
nsv5856020	copy number variation	1	nstd209	human		GRCh38 chr12: 236,123-240,356 , GRCh37.p13 chr12: 345,289-349,522	SLC6A13
nsv5850545	copy number variation	1	nstd209	human		GRCh38 chr12: 233,067-235,080 , GRCh37.p13 chr12: 342,233-344,246	SLC6A13
nsv5848516	copy number variation	1	nstd209	human		GRCh38 chr12: 222,455-224,654 , GRCh37.p13 chr12: 331,621-333,820	SLC6A13
nsv5847836	copy number variation	1	nstd209	human		GRCh38 chr12: 215,851-220,854 , GRCh37.p13 chr12: 325,017-330,020	SLC6A13

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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

Links from Gene

Items: 1 to 20 of 406

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Number of Variants: 20

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