dbVar for Gene (Select 107986407) - 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
nsv7098841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 10,149,255-18,180,300 , GRCh38.p12 chr5: 10,149,143-18,180,191	RN7SKP133, TAF11L1, 102 more genes
nsv7053949	inversion	1	nstd229	human		GRCh38 chr5: 12,599,104-19,642,739 , GRCh37.p13 chr5: 12,599,216-19,642,848	H3P18, H3P19, 86 more genes
nsv7049801	inversion	1	nstd229	human		GRCh38 chr5: 13,579,109-16,991,898 , GRCh37.p13 chr5: 13,579,218-16,992,007	MARCHF11-DT, OTULIN, 41 more genes
nsv7038701	inversion	1	nstd229	human		GRCh38 chr5: 12,558,868-18,815,622 , GRCh37.p13 chr5: 12,558,980-18,815,731	FBXL7, LINC02223, 81 more genes
nsv6776646	copy number variation	1	nstd229	human		GRCh38 chr5: 15,978,948-16,585,261 , GRCh37.p13 chr5: 15,979,057-16,585,370	MARCHF11, MARCHF11-AS1, 8 more genes
nsv6771215	copy number variation	1	nstd229	human		GRCh38 chr5: 16,127,571-16,133,982 , GRCh37.p13 chr5: 16,127,680-16,134,091	MARCHF11-AS1, MARCHF11
nsv6767645	copy number variation	1	nstd229	human		GRCh38 chr5: 16,122,764-16,126,978 , GRCh37.p13 chr5: 16,122,873-16,127,087	MARCHF11-AS1, MARCHF11
nsv6764289	copy number variation	1	nstd229	human		GRCh38 chr5: 16,140,187-16,151,858 , GRCh37.p13 chr5: 16,140,296-16,151,967	MARCHF11-AS1, MARCHF11
nsv6763133	copy number variation	1	nstd229	human		GRCh38 chr5: 16,124,702-16,125,379 , GRCh37.p13 chr5: 16,124,811-16,125,488	MARCHF11-AS1, MARCHF11
nsv6637149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861	LOC107986376, MARCHF11, 150 more genes
nsv6636942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932	LOC105374608, LSP1P3, 351 more genes
nsv6636849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678	ADCY2, HMGB3P3, 248 more genes
nsv6636672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743	LINC02123, LINC01020, 302 more genes
nsv6636606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420	BASP1, RNU1-76P, 338 more genes
nsv6569004	inversion	1	nstd223	human		GRCh38 chr5: 16,125,589-16,125,703 , GRCh37.p13 chr5: 16,125,698-16,125,812	MARCHF11-AS1, MARCHF11
nsv6393462	copy number variation	1	nstd223	human		GRCh38 chr5: 16,124,701-16,125,382 , GRCh37.p13 chr5: 16,124,810-16,125,491	MARCHF11, MARCHF11-AS1
nsv6382472	copy number variation	1	nstd223	human		GRCh38 chr5: 16,132,332-16,132,722 , GRCh37.p13 chr5: 16,132,441-16,132,831	MARCHF11-AS1, MARCHF11
nsv6381005	copy number variation	1	nstd223	human		GRCh38 chr5: 16,113,562-16,252,752 , GRCh37.p13 chr5: 16,113,671-16,252,861	MARCHF11-AS1, MARCHF11, 3 more genes
nsv6315441	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413	FBXL7, LOC105374608, 319 more genes
nsv6315416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269	LOC105374649, LINC02196, 333 more genes

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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 239

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Number of Variants: 20

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