dbVar for Gene (Select 8621) - 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
nsv7098120	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 39,990,241-40,041,650 , GRCh38.p12 chr7: 39,950,642-40,002,051	CDK13
nsv7097741	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,102,405-40,134,579 , GRCh38.p12 chr7: 40,062,806-40,094,980	CDK13
nsv7097625	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,027,178-40,134,579 , GRCh38.p12 chr7: 39,987,579-40,094,980	CDK13
nsv7097371	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,085,415-40,174,739 , GRCh38.p12 chr7: 40,045,816-40,135,140	SUGCT, HIGD1AP7, 2 more genes
nsv7097370	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 39,990,241-39,991,471 , GRCh38.p12 chr7: 39,950,642-39,951,872	CDK13
nsv6837978	copy number variation	1	nstd229	human		GRCh38 chr7: 39,815,544-39,999,163 , GRCh37.p13 chr7: 39,855,143-40,038,762	SSBP3P1, LOC100422519, 5 more genes
nsv6837775	copy number variation	1	nstd229	human		GRCh38 chr7: 39,957,205-40,115,607 , GRCh37.p13 chr7: 39,996,804-40,155,206	HIGD1AP7, CDK13
nsv6837574	copy number variation	1	nstd229	human		GRCh38 chr7: 40,082,682-40,152,007 , GRCh37.p13 chr7: 40,122,281-40,191,606	HIGD1AP7, CDK13, 3 more genes
nsv6837387	copy number variation	1	nstd229	human		GRCh38 chr7: 39,959,185-40,103,248 , GRCh37.p13 chr7: 39,998,784-40,142,847	CDK13
nsv6836605	copy number variation	1	nstd229	human		GRCh38 chr7: 40,067,024-40,071,100 , GRCh37.p13 chr7: 40,106,623-40,110,699	CDK13
nsv6836422	copy number variation	1	nstd229	human		GRCh38 chr7: 40,003,013-40,197,675 , GRCh37.p13 chr7: 40,042,612-40,237,274	SUGCT, HIGD1AP7, 3 more genes
nsv6836409	copy number variation	1	nstd229	human		GRCh38 chr7: 40,032,997-40,037,530 , GRCh37.p13 chr7: 40,072,596-40,077,129	CDK13
nsv6835519	copy number variation	1	nstd229	human		GRCh38 chr7: 39,994,481-40,142,869 , GRCh37.p13 chr7: 40,034,080-40,182,468	SUGCT, HIGD1AP7, 2 more genes
nsv6835334	copy number variation	1	nstd229	human		GRCh38 chr7: 40,045,980-40,200,368 , GRCh37.p13 chr7: 40,085,579-40,239,967	SUGCT, HIGD1AP7, 3 more genes
nsv6835101	copy number variation	1	nstd229	human		GRCh38 chr7: 40,001,113-40,166,645 , GRCh37.p13 chr7: 40,040,712-40,206,244	MPLKIP, CDK13, 3 more genes
nsv6834497	copy number variation	1	nstd229	human		GRCh38 chr7: 40,004,101-40,504,800 , GRCh37.p13 chr7: 40,043,700-40,544,399	MPLKIP, HIGD1AP7, 4 more genes
nsv6834393	copy number variation	1	nstd229	human		GRCh38 chr7: 38,944,248-39,960,814 , GRCh37.p13 chr7: 38,983,848-40,000,413	LOC100422519, LOC646999, 21 more genes
nsv6833984	copy number variation	1	nstd229	human		GRCh38 chr7: 40,095,253-40,262,079 , GRCh37.p13 chr7: 40,134,852-40,301,678	THUMPD3P1, SUGCT, 4 more genes
nsv6833715	copy number variation	1	nstd229	human		GRCh38 chr7: 39,962,543-40,108,168 , GRCh37.p13 chr7: 40,002,142-40,147,767	CDK13
nsv6833701	copy number variation	1	nstd229	human		GRCh38 chr7: 40,028,798-40,037,265 , GRCh37.p13 chr7: 40,068,397-40,076,864	CDK13

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 621

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Number of Variants: 20

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