dbVar for Gene (Select 414) - 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
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
nsv7098619	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 2,835,825-2,878,441 , GRCh38.p12 chrX: 2,917,784-2,960,400	ARSL, ARSD
nsv7098018	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 2,838,622-2,878,441 , GRCh38.p12 chrX: 2,920,581-2,960,400	ARSL, ARSD
nsv7077989	copy number variation	1	nstd229	human		GRCh38 chrX: 2,924,256-2,948,578 , GRCh37.p13 chrX: 2,842,297-2,866,619	ARSL, ARSD
nsv7077536	copy number variation	1	nstd229	human		GRCh38 chrX: 2,902,501-2,968,700 , GRCh37.p13 chrX: 2,820,542-2,886,741	ARSD, ARSL, 1 more genes
nsv7075795	copy number variation	1	nstd229	human		GRCh38 chrX: 2,908,031-2,908,132 , GRCh37.p13 chrX: 2,826,072-2,826,173	ARSD
nsv7070822	copy number variation	1	nstd229	human		GRCh38 chrX: 2,921,202-2,921,307 , GRCh37.p13 chrX: 2,839,243-2,839,348	ARSD
nsv7070208	copy number variation	1	nstd229	human		GRCh38 chrX: 2,904,940-2,906,486 , GRCh37.p13 chrX: 2,822,981-2,824,527	ARSD-AS1, ARSD
nsv7069272	copy number variation	1	nstd229	human		GRCh38 chrX: 2,927,075-2,932,170 , GRCh37.p13 chrX: 2,845,116-2,850,211	ARSD
nsv7068773	copy number variation	1	nstd229	human		GRCh38 chrX: 2,912,462-3,098,590 , GRCh37.p13 chrX: 2,830,503-3,016,631	ARSF, RN7SL578P, 3 more genes
nsv7067136	copy number variation	1	nstd229	human		GRCh38 chrX: 2,923,484-2,927,807 , GRCh37.p13 chrX: 2,841,525-2,845,848	ARSD
nsv7065031	copy number variation	1	nstd229	human		GRCh38 chrX: 2,885,751-2,906,250 , GRCh37.p13 chrX: 2,803,792-2,824,291	ARSD, ARSD-AS1
nsv7064625	copy number variation	1	nstd229	human		GRCh38 chrX: 2,911,258-2,915,883 , GRCh37.p13 chrX: 2,829,299-2,833,924	ARSD
nsv7062389	copy number variation	1	nstd229	human		GRCh38 chrX: 2,914,740-2,923,232 , GRCh37.p13 chrX: 2,832,781-2,841,273	ARSD
nsv6636165	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899	GPX1P1, XG, 108 more genes
nsv6636134	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 2,370,150-3,027,737 , GRCh38.p12 chrX: 2,452,109-3,109,696	ZBED1, CD99P1, 13 more genes
nsv6636115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 2,703,823-3,354,304 , GRCh38.p12 chrX: 2,785,782-3,436,263	LINC01546, MXRA5, 9 more genes
nsv6636029	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 1,626,596-7,832,236 , GRCh38.p12 chrX: 1,507,703-7,864,195	ARSL, FAM239A, 53 more genes
nsv6635989	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 1,932,788-9,676,331 , GRCh38.p12 chrX: 1,813,895-9,708,291	STS, ARSD, 67 more genes

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Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 503

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Number of Variants: 20

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