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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146774insertion1nstd232human GRCh37.p13 chr12: 98,993,905-98,993,905 , GRCh38.p12 chr12: 98,600,127-98,600,127 SLC25A3, SNORA53
    nsv7142317copy number variation1nstd232human GRCh37.p13 chr12: 98,995,057-98,995,142 , GRCh38.p12 chr12: 98,601,279-98,601,364 SLC25A3
    nsv7094157copy number variation1nstd102humanUncertain significance GRCh37 chr12: 98,987,757-98,995,306 , GRCh38.p12 chr12: 98,593,979-98,601,528 SLC25A3, SNORA53
    nsv7073020inversion1nstd229human GRCh38 chr12: 96,481,691-98,593,227 , GRCh37.p13 chr12: 96,875,469-98,987,005 TRW-CCA4-1, LINC02409, 26 more genes
    nsv7071764inversion1nstd229human GRCh38 chr12: 97,813,083-99,306,980 , GRCh37.p13 chr12: 98,206,861-99,700,758 TRW-CCA4-1, PPIAP8, 18 more genes
    nsv7062523inversion1nstd229human GRCh38 chr12: 97,595,549-99,328,182 , GRCh37.p13 chr12: 97,989,327-99,721,960 RNU4-41P, MIR4303, 20 more genes
    nsv6928788copy number variation1nstd229human GRCh38 chr12: 98,538,101-98,594,600 , GRCh37.p13 chr12: 98,931,879-98,988,378 SLC25A3, PPIAP8, 1 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6919247copy number variation1nstd229human GRCh38 chr12: 98,594,773-98,595,287 , GRCh37.p13 chr12: 98,988,551-98,989,065 SLC25A3
    nsv6919052copy number variation1nstd229human GRCh38 chr12: 98,600,525-98,625,089 , GRCh37.p13 chr12: 98,994,303-99,018,867 SLC25A3, IKBIP
    nsv6621763copy number variation1nstd224human GRCh37 chr12: 98,927,984-99,020,453 , GRCh38.p12 chr12: 98,534,206-98,626,675 PPIAP8, SNORA53, 3 more genes
    nsv6591260inversion1nstd223human GRCh38 chr12: 98,596,965-98,597,465 , GRCh37.p13 chr12: 98,990,743-98,991,243 SLC25A3
    nsv6590693inversion1nstd223human GRCh38 chr12: 97,813,083-99,306,980 , GRCh37.p13 chr12: 98,206,861-99,700,758 TRW-CCA4-1, PPIAP8, 18 more genes
    nsv6586137inversion1nstd223human GRCh38 chr12: 98,592,054-98,592,577 , GRCh37.p13 chr12: 98,985,832-98,986,355 SLC25A3
    nsv6463540copy number variation1nstd223human GRCh38 chr12: 98,575,806-98,685,404 , GRCh37.p13 chr12: 98,969,584-99,079,182 PPIAP8, SLC25A3, 3 more genes
    nsv6463062copy number variation1nstd223human GRCh38 chr12: 98,588,101-98,593,100 , GRCh37.p13 chr12: 98,981,879-98,986,878 SLC25A3, PPIAP8
    nsv6248496mobile element insertion1nstd215human GRCh38 chr12: 98,606,550-98,606,550 , GRCh37.p13 chr12: 99,000,328-99,000,328 SLC25A3
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132623copy number variation1nstd213human GRCh37 chr12: 98,530,000-99,850,001 , GRCh38.p12 chr12: 98,136,222-99,456,223 ANKS1B, SLC9A7P1, 16 more genes
    nsv6132521copy number variation1nstd213human GRCh37 chr12: 97,760,000-100,480,001 , GRCh38.p12 chr12: 97,366,222-100,086,223 TMPO, ANKS1B, 26 more genes
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