dbVar for Gene (Select 55796) - 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
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
nsv7083916	copy number variation	1	nstd229	human		GRCh38 chrX: 132,486,101-132,488,900 , GRCh37.p13 chrX: 131,620,129-131,622,928	MBNL3
nsv7083915	copy number variation	1	nstd229	human		GRCh38 chrX: 132,485,607-132,510,264 , GRCh37.p13 chrX: 131,619,635-131,644,292	MBNL3
nsv7083914	copy number variation	1	nstd229	human		GRCh38 chrX: 132,470,969-132,475,192 , GRCh37.p13 chrX: 131,604,997-131,609,220	MBNL3
nsv7083913	copy number variation	1	nstd229	human		GRCh38 chrX: 132,466,857-132,467,270 , GRCh37.p13 chrX: 131,600,885-131,601,298	MBNL3
nsv7083912	copy number variation	1	nstd229	human		GRCh38 chrX: 132,464,184-132,464,364 , GRCh37.p13 chrX: 131,598,212-131,598,392	MBNL3
nsv7083911	copy number variation	1	nstd229	human		GRCh38 chrX: 132,463,667-132,464,190 , GRCh37.p13 chrX: 131,597,695-131,598,218	MBNL3
nsv7083910	copy number variation	1	nstd229	human		GRCh38 chrX: 132,446,534-132,447,087 , GRCh37.p13 chrX: 131,580,562-131,581,115	MBNL3
nsv7083909	copy number variation	1	nstd229	human		GRCh38 chrX: 132,417,286-132,442,955 , GRCh37.p13 chrX: 131,551,314-131,576,983	RAP2C-AS1, MBNL3
nsv7083908	copy number variation	1	nstd229	human		GRCh38 chrX: 132,413,290-132,423,290 , GRCh37.p13 chrX: 131,547,318-131,557,318	MBNL3, RAP2C-AS1
nsv7083907	copy number variation	1	nstd229	human		GRCh38 chrX: 132,406,708-132,406,932 , GRCh37.p13 chrX: 131,540,736-131,540,960	MBNL3, RAP2C-AS1
nsv7083906	copy number variation	1	nstd229	human		GRCh38 chrX: 132,406,187-132,406,550 , GRCh37.p13 chrX: 131,540,215-131,540,578	MBNL3, RAP2C-AS1
nsv7083905	copy number variation	1	nstd229	human		GRCh38 chrX: 132,393,101-132,417,800 , GRCh37.p13 chrX: 131,527,129-131,551,828	MBNL3, RAP2C-AS1
nsv7083904	copy number variation	1	nstd229	human		GRCh38 chrX: 132,391,001-132,402,600 , GRCh37.p13 chrX: 131,525,029-131,536,628	MBNL3, RAP2C-AS1
nsv7083903	copy number variation	1	nstd229	human		GRCh38 chrX: 132,390,901-132,402,900 , GRCh37.p13 chrX: 131,524,929-131,536,928	MBNL3, RAP2C-AS1
nsv7083902	copy number variation	1	nstd229	human		GRCh38 chrX: 132,390,701-132,417,700 , GRCh37.p13 chrX: 131,524,729-131,551,728	RAP2C-AS1, MBNL3
nsv7083901	copy number variation	1	nstd229	human		GRCh38 chrX: 132,389,488-132,389,556 , GRCh37.p13 chrX: 131,523,516-131,523,584	MBNL3, RAP2C-AS1
nsv7083900	copy number variation	1	nstd229	human		GRCh38 chrX: 132,379,580-132,403,492 , GRCh37.p13 chrX: 131,513,608-131,537,520	MBNL3, RAP2C-AS1
nsv7083899	copy number variation	1	nstd229	human		GRCh38 chrX: 132,375,241-132,375,594 , GRCh37.p13 chrX: 131,509,269-131,509,622	MBNL3, RAP2C-AS1
nsv7083898	copy number variation	1	nstd229	human		GRCh38 chrX: 132,369,501-132,408,000 , GRCh37.p13 chrX: 131,503,529-131,542,028	MBNL3, RAP2C-AS1

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 440

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Number of Variants: 20

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