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Items: 1 to 20 of 764

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057990inversion1nstd229human GRCh38 chr6: 63,423,586-63,424,491 , GRCh37.p13 chr6: 64,133,491-64,134,396 LGSN
    nsv7056256inversion1nstd229human GRCh38 chr6: 63,528,149-63,539,254 , GRCh37.p13 chr6: 64,238,054-64,249,159 PTP4A1, LGSN
    nsv7053351inversion1nstd229human GRCh38 chr6: 62,782,490-63,283,394 , GRCh37.p13 chr6: 63,492,395-63,993,299 LOC442225, FKBP1C, 3 more genes
    nsv7052688inversion1nstd229human GRCh38 chr6: 63,534,001-63,539,146 , GRCh37.p13 chr6: 64,243,906-64,249,051 PTP4A1, LGSN
    nsv7048701inversion1nstd229human GRCh38 chr6: 63,342,252-63,349,958 , GRCh37.p13 chr6: 64,052,157-64,059,863 LGSN
    nsv7047612inversion1nstd229human GRCh38 chr6: 63,480,476-63,510,632 , GRCh37.p13 chr6: 64,190,381-64,220,537 EEF1B2P5, LGSN
    nsv7043671inversion1nstd229human GRCh38 chr6: 62,662,016-67,126,368 , GRCh37.p13 chr6: 63,371,921-67,836,261 LOC105377841, EEF1B2P5, 31 more genes
    nsv7043156inversion1nstd229human GRCh38 chr6: 63,481,792-63,519,384 , GRCh37.p13 chr6: 64,191,697-64,229,289 LGSN, EEF1B2P5
    nsv7039203inversion1nstd229human GRCh38 chr6: 63,532,246-64,407,678 , GRCh37.p13 chr6: 64,242,151-65,117,571 LOC100422587, LOC107986608, 9 more genes
    nsv6797976copy number variation1nstd229human GRCh38 chr6: 63,488,822-63,493,060 , GRCh37.p13 chr6: 64,198,727-64,202,965 LGSN
    nsv6796949copy number variation1nstd229human GRCh38 chr6: 63,297,136-63,302,088 , GRCh37.p13 chr6: 64,007,041-64,011,993 LGSN
    nsv6796030copy number variation1nstd229human GRCh38 chr6: 63,547,556-63,551,083 , GRCh37.p13 chr6: 64,257,461-64,260,988 PTP4A1, LGSN, 1 more genes
    nsv6795394copy number variation1nstd229human GRCh38 chr6: 63,355,901-63,361,600 , GRCh37.p13 chr6: 64,065,806-64,071,505 LGSN
    nsv6795200copy number variation1nstd229human GRCh38 chr6: 63,357,501-63,359,900 , GRCh37.p13 chr6: 64,067,406-64,069,805 LGSN
    nsv6795019copy number variation1nstd229human GRCh38 chr6: 63,377,601-63,489,700 , GRCh37.p13 chr6: 64,087,506-64,199,605 EEF1B2P5, LGSN, 2 more genes
    nsv6794287copy number variation1nstd229human GRCh38 chr6: 63,419,742-63,421,210 , GRCh37.p13 chr6: 64,129,647-64,131,115 LGSN
    nsv6793883copy number variation1nstd229human GRCh38 chr6: 63,556,819-63,559,276 , GRCh37.p13 chr6: 64,266,724-64,269,181 PTP4A1, LGSN
    nsv6793233copy number variation1nstd229human GRCh38 chr6: 63,544,205-63,544,241 , GRCh37.p13 chr6: 64,254,110-64,254,146 LGSN, PTP4A1
    nsv6792946copy number variation1nstd229human GRCh38 chr6: 63,554,301-63,567,100 , GRCh37.p13 chr6: 64,264,206-64,277,005 LGSN, PTP4A1
    nsv6792741copy number variation1nstd229human GRCh38 chr6: 63,531,667-63,537,348 , GRCh37.p13 chr6: 64,241,572-64,247,253 PTP4A1, LGSN
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