dbVar for Gene (Select 4611) - 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
nsv7098108	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 106,456,106-106,959,200 , GRCh38.p12 chrX: 107,212,876-107,715,970	TSC22D3, DNAAF6, 6 more genes
nsv7098107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020	VSIG1, NXT2, 32 more genes
nsv7078276	copy number variation	1	nstd229	human		GRCh38 chrX: 107,271,801-107,274,100 , GRCh37.p13 chrX: 106,515,031-106,517,330	MYCLP1
nsv7078275	copy number variation	1	nstd229	human		GRCh38 chrX: 107,270,201-107,274,100 , GRCh37.p13 chrX: 106,513,431-106,517,330	MYCLP1
nsv7078271	copy number variation	1	nstd229	human		GRCh38 chrX: 107,187,454-107,396,128 , GRCh37.p13 chrX: 106,430,684-106,639,358	MYCLP1, DNAAF6, 2 more genes
nsv7078270	copy number variation	1	nstd229	human		GRCh38 chrX: 107,187,351-107,398,286 , GRCh37.p13 chrX: 106,430,581-106,641,516	DNAAF6, MYCLP1, 2 more genes
nsv7078262	copy number variation	1	nstd229	human		GRCh38 chrX: 107,064,984-107,532,736 , GRCh37.p13 chrX: 106,308,214-106,775,966	FRMPD3-AS1, FRMPD3, 7 more genes
nsv7052621	inversion	1	nstd229	human		GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650	CSGALNACT2P2, LOC107985662, 82 more genes
nsv7044993	inversion	1	nstd229	human		GRCh38 chrX: 104,618,913-113,302,073 , GRCh37.p13 chrX: 103,863,594-112,545,300	NCBP2L, TEX13B, 92 more genes
nsv7041719	inversion	1	nstd229	human		GRCh38 chrX: 105,592,744-110,464,662 , GRCh37.p13 chrX: 104,836,737-109,707,890	LOC105373312, PPP6CP, 59 more genes
nsv6637086	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 106,420,267-106,625,135 , GRCh38.p12 chrX: 107,177,037-107,381,905	NUP62CL, MYCLP1, 2 more genes
nsv6636905	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 105,730,612-107,162,289 , GRCh38.p12 chrX: 106,487,382-107,919,059	NUP62CL, MID2, 21 more genes
nsv6636543	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366	TRPC5OS, LOC105373314, 351 more genes
nsv6634329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930	NXF4, RHOXF1P1, 489 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
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

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Items: 1 to 20 of 308

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Number of Variants: 20

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