dbVar for Gene (Select 959) - 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
nsv7098346	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 135,730,408-135,741,574 , GRCh38.p12 chrX: 136,648,249-136,659,415	CD40LG
nsv7097991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 135,730,408-136,113,833 , GRCh38.p12 chrX: 136,648,249-137,031,674	RPL7P56, RAB28P5, 11 more genes
nsv7084306	copy number variation	1	nstd229	human		GRCh38 chrX: 136,659,728-136,659,950 , GRCh37.p13 chrX: 135,741,887-135,742,109	CD40LG
nsv7084305	copy number variation	1	nstd229	human		GRCh38 chrX: 136,651,672-136,652,052 , GRCh37.p13 chrX: 135,733,831-135,734,211	CD40LG
nsv7084304	copy number variation	1	nstd229	human		GRCh38 chrX: 136,647,603-136,647,773 , GRCh37.p13 chrX: 135,729,762-135,729,932	CD40LG
nsv7084303	copy number variation	1	nstd229	human		GRCh38 chrX: 136,622,176-137,342,517 , GRCh37.p13 chrX: 135,704,335-136,424,676	RPL7P56, RAB28P5, 12 more genes
nsv7084302	copy number variation	1	nstd229	human		GRCh38 chrX: 136,614,398-136,681,354 , GRCh37.p13 chrX: 135,696,557-135,763,513	CD40LG, ARHGEF6, 1 more genes
nsv7084288	copy number variation	1	nstd229	human		GRCh38 chrX: 136,430,040-137,211,313 , GRCh37.p13 chrX: 135,512,199-136,293,472	VGLL1, GPR101, 17 more genes
nsv7045875	inversion	1	nstd229	human		GRCh38 chrX: 136,652,264-136,657,204 , GRCh37.p13 chrX: 135,734,423-135,739,363	CD40LG
nsv6636407	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066	RN7SKP31, LOC728470, 539 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
nsv6633775	copy number variation	1	nstd224	human		GRCh37 chrX: 133,906,202-135,831,362 , GRCh38.p12 chrX: 134,772,172-136,749,203	GAPDHP67, VGLL1, 63 more genes
nsv6315429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066	H2AB1, GPR174, 1081 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
nsv6315389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066	RBMX, LOC100129144, 2042 more genes
nsv6315332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066	MAGT1, TAFAZZIN, 1337 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
nsv6313141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 135,730,388-135,737,600 , GRCh38.p12 chrX: 136,648,229-136,655,441	CD40LG
nsv6313037	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chrX: 135,067,662-136,652,229 , GRCh38.p12 chrX: 135,985,503-137,570,070	GPR101, SRRM1P3, 26 more genes

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Items: 1 to 20 of 288

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Number of Variants: 20

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