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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099204copy number variation1nstd231human GRCh38.p12 chr1: 51,433,462-53,162,521 , GRCh37 chr1: 51,899,134-53,628,193 EPS15, GPX7, 53 more genes
    nsv7096055copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,407,448-53,407,545 , GRCh38.p12 chr1: 52,941,776-52,941,873 H3P2, SCP2
    nsv7095624copy number variation1nstd102humanUncertain significance GRCh37 chr1: 53,413,661-53,516,376 , GRCh38.p12 chr1: 52,947,989-53,050,704 SCP2, RRAS2P1, 1 more genes
    nsv7095623copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,407,448-53,446,235 , GRCh38.p12 chr1: 52,941,776-52,980,563 H3P2, SCP2
    nsv7095622copy number variation1nstd102humanUncertain significance GRCh37 chr1: 53,393,069-53,420,496 , GRCh38.p12 chr1: 52,927,397-52,954,824 SCP2, ECHDC2, 1 more genes
    nsv7057303inversion1nstd229human GRCh38 chr1: 53,024,827-53,027,193 , GRCh37.p13 chr1: 53,490,499-53,492,865 SCP2
    nsv7052979inversion1nstd229human GRCh38 chr1: 52,902,490-52,926,550 , GRCh37.p13 chr1: 53,368,162-53,392,222 LOC112268226, SCP2, 2 more genes
    nsv7052650inversion1nstd229human GRCh38 chr1: 47,584,744-54,395,558 , GRCh37.p13 chr1: 48,050,416-54,861,231 ANAPC10P1, SPATA6, 137 more genes
    nsv7051144inversion1nstd229human GRCh38 chr1: 52,995,523-53,296,653 , GRCh37.p13 chr1: 53,461,195-53,762,325 MAGOH, LOC105378724, 12 more genes
    nsv7050595inversion1nstd229human GRCh38 chr1: 52,984,512-52,995,528 , GRCh37.p13 chr1: 53,450,184-53,461,200 SCP2, RRAS2P1, 1 more genes
    nsv7047407inversion1nstd229human GRCh38 chr1: 52,902,579-52,926,515 , GRCh37.p13 chr1: 53,368,251-53,392,187 ECHDC2, SCP2, 2 more genes
    nsv7046046inversion1nstd229human GRCh38 chr1: 52,975,893-52,983,183 , GRCh37.p13 chr1: 53,441,565-53,448,855 SCP2
    nsv6651663copy number variation1nstd229human GRCh38 chr1: 52,980,187-53,069,868 , GRCh37.p13 chr1: 53,445,859-53,535,540 PODN, SCP2, 2 more genes
    nsv6651662copy number variation1nstd229human GRCh38 chr1: 52,946,337-52,946,471 , GRCh37.p13 chr1: 53,412,009-53,412,143 SCP2
    nsv6651656copy number variation1nstd229human GRCh38 chr1: 52,777,527-53,016,476 , GRCh37.p13 chr1: 53,243,199-53,482,148 RNU6-969P, H3P2, 8 more genes
    nsv6651573copy number variation1nstd229human GRCh38 chr1: 53,036,953-53,037,852 , GRCh37.p13 chr1: 53,502,625-53,503,524 SCP2
    nsv6651572copy number variation1nstd229human GRCh38 chr1: 52,951,133-52,956,785 , GRCh37.p13 chr1: 53,416,805-53,422,457 SCP2
    nsv6651571copy number variation1nstd229human GRCh38 chr1: 52,932,246-52,983,264 , GRCh37.p13 chr1: 53,397,918-53,448,936 SCP2, H3P2
    nsv6651447copy number variation1nstd229human GRCh38 chr1: 53,051,452-53,057,751 , GRCh37.p13 chr1: 53,517,124-53,523,423 SCP2
    nsv6651446copy number variation1nstd229human GRCh38 chr1: 53,038,236-53,038,267 , GRCh37.p13 chr1: 53,503,908-53,503,939 SCP2
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