dbVar for Gene (Select 6473) - 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
nsv7138010	copy number variation	1	nstd232	human		GRCh37.p13 chrX: 604,704-604,758 , GRCh38.p12 chrX: 643,969-644,023	SHOX
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
nsv7137010	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 585,078-601,555 , GRCh38.p12 chrX: 624,343-640,820	SHOX
nsv7098867	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773	RPL14P5, NLGN4X, 64 more genes
nsv6636179	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 168,547-1,536,716 , GRCh38.p12 chrX: 251,880-1,417,823	LOC100418703, PLCXD1, 19 more genes
nsv6636090	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 201,705-2,696,762 , GRCh38.p12 chrX: 285,038-2,778,721	ASMT, LINC00685, 33 more genes
nsv6636040	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 565,816-1,356,042 , GRCh38.p12 chrX: 605,081-1,237,149	LOC652608, SHOX, 3 more genes
nsv6634242	copy number variation	1	nstd224	human		GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895	NR0B1, ALAS2, 2154 more genes
nsv6634094	copy number variation	4	nstd224	human		GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415	ASMT, ASS1P6, 570 more genes
nsv6315577	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608	ACTG1P10, NR0B1, 778 more genes
nsv6315454	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-10,368,820 , GRCh38.p12 chrX: 251,879-10,400,780	LOC107985675, PRKX-AS1, 101 more genes
nsv6315430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-11,080,743 , GRCh38.p12 chrX: 251,879-11,062,623	RPS27AP20, PPP2R3B, 103 more genes
nsv6315396	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 566,009-1,262,195 , GRCh38.p12 chrX: 605,274-1,162,042	LOC100418703, SHOX, 1 more genes
nsv6315393	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383	H2BP8, LOC101060199, 2151 more genes
nsv6315385	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 416,347-1,993,495 , GRCh38.p12 chrX: 455,612-1,874,602	FABP5P13, LOC652608, 20 more genes
nsv6315378	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 566,009-1,356,042 , GRCh38.p12 chrX: 605,274-1,237,149	SHOX, CRLF2, 3 more genes
nsv6315377	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrY: 516,009-1,306,042 , GRCh38.p12 chrY: 605,274-1,237,149	LOC652608, LOC100418703, 3 more genes
nsv6315331	copy number variation	4	nstd102	human	Pathogenic	GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895	PLAC1, PGK1P1, 2154 more genes
nsv6315330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871	NPM1P9, UBE2E4P, 799 more genes
nsv6315262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 372,029-1,262,195 , GRCh38.p12 chrX: 411,294-1,162,042	SHOX, RPL14P5, 4 more genes

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Object Type

Organism

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Has Clinical Interpretation

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Items: 1 to 20 of 965

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Number of Variants: 20

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