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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904011copy number variation1nstd209human GRCh38 chr3: 100,289,472-100,332,840 , GRCh37.p13 chr3: 100,008,316-100,051,684 NIT2, TBC1D23
    nsv5450858copy number variation1nstd206human GRCh38 chr3: 100,337,655-100,347,383 , GRCh37.p13 chr3: 100,056,499-100,066,227 NIT2
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4919166copy number variation1nstd200human GRCh38 chr3: 100,336,855-100,342,506 , GRCh37.p13 chr3: 100,055,699-100,061,350 NIT2
    nsv4914554copy number variation1nstd200human GRCh38 chr3: 100,188,066-100,400,094 , GRCh37.p13 chr3: 99,906,910-100,118,938 TOMM70, NIT2, 5 more genes
    nsv4887622inversion1nstd200human GRCh37 chr3: 94,357,590-100,127,961 , GRCh38.p12 chr3: 94,638,746-100,409,117 , CPOX, 82 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797683copy number variation1nstd200human GRCh37 chr3: 100,055,699-100,061,350 , GRCh38.p12 chr3: 100,336,855-100,342,506 NIT2
    nsv4794240copy number variation1nstd200human GRCh37 chr3: 100,008,316-100,051,685 , GRCh38.p12 chr3: 100,289,472-100,332,841 TBC1D23, NIT2
    nsv4728581copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 95,563,096-102,371,126 , GRCh38.p12 chr3: 95,844,252-102,652,282 COL8A1, CPOX, 107 more genes
    nsv4586970copy number variation1nstd183human GRCh37 chr3: 100,079,007-100,095,172 , GRCh38.p12 chr3: 100,360,163-100,376,328 NIT2, TOMM70
    nsv4073890copy number variation1nstd166human GRCh37.p13 chr3: 100,008,316-100,051,685 , GRCh38.p12 chr3: 100,289,472-100,332,841 TBC1D23, NIT2
    nsv4073501copy number variation1nstd166human GRCh37.p13 chr3: 100,055,700-100,061,349 , GRCh38.p12 chr3: 100,336,856-100,342,505 NIT2
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
    nsv3916416copy number variation1nstd102humanUncertain significance GRCh37 chr3: 99,478,229-100,124,625 , GRCh38 chr3: 99,759,385-100,405,781 , NCBI36 chr3: 100,960,919-101,607,315 TMEM30CP, LOC105374010, 13 more genes
    nsv3911724copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749 COL8A1, CPOX, 132 more genes
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