dbVar for Gene (Select 554203) - 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
nsv7137157	inversion	1	nstd234	human		GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132	ABCB7, ACTG1P10, 775 more genes
nsv7137063	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409	RN7SL581P, HMGB1P32, 2151 more genes
nsv7092477	copy number variation	1	nstd229	human		GRCh38 chrX: 74,069,021-74,074,999 , GRCh37.p13 chrX: 73,288,856-73,294,834	FTX, JPX
nsv7092476	copy number variation	1	nstd229	human		GRCh38 chrX: 74,065,568-74,065,923 , GRCh37.p13 chrX: 73,285,403-73,285,758	FTX, SHISA5P2, 1 more genes
nsv7092475	copy number variation	1	nstd229	human		GRCh38 chrX: 74,059,985-74,066,489 , GRCh37.p13 chrX: 73,279,820-73,286,324	SHISA5P2, JPX, 1 more genes
nsv7092474	copy number variation	1	nstd229	human		GRCh38 chrX: 74,055,006-74,196,411 , GRCh37.p13 chrX: 73,274,841-73,416,246	DDX3P1, DDX3P2, 7 more genes
nsv7092473	copy number variation	1	nstd229	human		GRCh38 chrX: 74,042,453-74,202,599 , GRCh37.p13 chrX: 73,262,288-73,422,434	JPX, ATP5MKP1, 8 more genes
nsv7092472	copy number variation	1	nstd229	human		GRCh38 chrX: 74,037,401-74,041,700 , GRCh37.p13 chrX: 73,257,236-73,261,535	FTX, JPX
nsv7092471	copy number variation	1	nstd229	human		GRCh38 chrX: 74,032,491-74,032,889 , GRCh37.p13 chrX: 73,252,326-73,252,724	FTX, JPX
nsv7092470	copy number variation	1	nstd229	human		GRCh38 chrX: 74,023,499-74,070,495 , GRCh37.p13 chrX: 73,243,334-73,290,330	FTX, SHISA5P2, 2 more genes
nsv7092469	copy number variation	1	nstd229	human		GRCh38 chrX: 74,019,810-74,163,082 , GRCh37.p13 chrX: 73,239,645-73,382,917	DDX3P2, FTX, 6 more genes
nsv7092468	copy number variation	1	nstd229	human		GRCh38 chrX: 74,014,484-74,014,601 , GRCh37.p13 chrX: 73,234,319-73,234,436	JPX
nsv7092467	copy number variation	1	nstd229	human		GRCh38 chrX: 74,009,520-74,009,695 , GRCh37.p13 chrX: 73,229,355-73,229,530	JPX
nsv7092466	copy number variation	1	nstd229	human		GRCh38 chrX: 73,989,249-73,989,445 , GRCh37.p13 chrX: 73,209,084-73,209,280	JPX
nsv7092465	copy number variation	1	nstd229	human		GRCh38 chrX: 73,986,150-73,990,970 , GRCh37.p13 chrX: 73,205,985-73,210,805	JPX
nsv7092464	copy number variation	1	nstd229	human		GRCh38 chrX: 73,984,106-73,987,002 , GRCh37.p13 chrX: 73,203,941-73,206,837	JPX
nsv7092463	copy number variation	1	nstd229	human		GRCh38 chrX: 73,981,388-73,991,332 , GRCh37.p13 chrX: 73,201,223-73,211,167	JPX
nsv7092462	copy number variation	1	nstd229	human		GRCh38 chrX: 73,981,317-73,983,630 , GRCh37.p13 chrX: 73,201,152-73,203,465	JPX
nsv7092461	copy number variation	1	nstd229	human		GRCh38 chrX: 73,974,299-73,976,816 , GRCh37.p13 chrX: 73,194,134-73,196,651	JPX
nsv7092460	copy number variation	1	nstd229	human		GRCh38 chrX: 73,954,101-73,957,100 , GRCh37.p13 chrX: 73,173,936-73,176,935	JPX

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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 500

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Number of Variants: 20

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Supplemental Content

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Recent activity