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Items: 1 to 20 of 593

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098593copy number variation1nstd102humanPathogenic GRCh37 chrX: 14,875,974-14,891,184 , GRCh38.p12 chrX: 14,857,852-14,873,062 FANCB, MOSPD2
    nsv7098592copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 14,861,689-15,870,650 , GRCh38.p12 chrX: 14,843,567-15,852,527 VEGFD, CA5BP1-CA5B, 20 more genes
    nsv7098591copy number variation1nstd102humanUncertain significance GRCh37 chrX: 14,861,689-14,877,476 , GRCh38.p12 chrX: 14,843,567-14,859,354 FANCB
    nsv7098231copy number variation1nstd102humanPathogenic GRCh37 chrX: 14,861,689-14,891,184 , GRCh38.p12 chrX: 14,843,567-14,873,062 MOSPD2, FANCB
    nsv7085239copy number variation1nstd229human GRCh38 chrX: 14,831,864-14,854,212 , GRCh37.p13 chrX: 14,849,986-14,872,334 NPM1P9, FANCB
    nsv7085225copy number variation1nstd229human GRCh38 chrX: 14,820,378-14,825,240 , GRCh37.p13 chrX: 14,838,500-14,843,362 FANCB
    nsv7085194copy number variation1nstd229human GRCh38 chrX: 14,793,738-14,793,838 , GRCh37.p13 chrX: 14,811,860-14,811,960 FANCB
    nsv7085191copy number variation1nstd229human GRCh38 chrX: 14,789,301-14,793,200 , GRCh37.p13 chrX: 14,807,423-14,811,322 FANCB
    nsv7085186copy number variation1nstd229human GRCh38 chrX: 14,783,968-14,805,701 , GRCh37.p13 chrX: 14,802,090-14,823,823 FANCB
    nsv7085183copy number variation1nstd229human GRCh38 chrX: 14,779,643-14,781,289 , GRCh37.p13 chrX: 14,797,765-14,799,411 FANCB
    nsv7085151copy number variation1nstd229human GRCh38 chrX: 14,755,925-14,768,855 , GRCh37.p13 chrX: 14,774,047-14,786,977 FANCB
    nsv7085138copy number variation1nstd229human GRCh38 chrX: 14,749,352-14,749,541 , GRCh37.p13 chrX: 14,767,474-14,767,663 FANCB
    nsv7085132copy number variation1nstd229human GRCh38 chrX: 14,747,159-14,747,783 , GRCh37.p13 chrX: 14,765,281-14,765,905 FANCB
    nsv7085123copy number variation1nstd229human GRCh38 chrX: 14,744,183-14,751,626 , GRCh37.p13 chrX: 14,762,305-14,769,748 FANCB
    nsv7085111copy number variation1nstd229human GRCh38 chrX: 14,732,566-14,747,867 , GRCh37.p13 chrX: 14,750,688-14,765,989 FANCB
    nsv7085086copy number variation1nstd229human GRCh38 chrX: 14,710,198-14,710,492 , GRCh37.p13 chrX: 14,728,320-14,728,614 GLRA2, FANCB
    nsv7085079copy number variation1nstd229human GRCh38 chrX: 14,706,062-14,706,110 , GRCh37.p13 chrX: 14,724,184-14,724,232 GLRA2, FANCB
    nsv7085076copy number variation1nstd229human GRCh38 chrX: 14,704,701-14,707,700 , GRCh37.p13 chrX: 14,722,823-14,725,822 FANCB, GLRA2
    nsv7085068copy number variation1nstd229human GRCh38 chrX: 14,700,466-14,701,953 , GRCh37.p13 chrX: 14,718,588-14,720,075 GLRA2, FANCB
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