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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097559copy number variation1nstd102humanUncertain significance GRCh37 chr6: 100,040,906-100,057,203 , GRCh38.p12 chr6: 99,593,030-99,609,327 PRDM13
    nsv7097304copy number variation1nstd102humanPathogenic GRCh37 chr6: 100,040,906-100,062,635 , GRCh38.p12 chr6: 99,593,030-99,614,759 PRDM13
    nsv7042952inversion1nstd229human GRCh38 chr6: 99,567,141-99,930,538 , GRCh37.p13 chr6: 100,015,017-100,378,414 RPS3P5, CCNC, 3 more genes
    nsv6811140copy number variation1nstd229human GRCh38 chr6: 97,373,758-103,907,621 , GRCh37.p13 chr6: 97,821,634-104,355,496 FBXL4, PRDM13, 37 more genes
    nsv6808494copy number variation1nstd229human GRCh38 chr6: 99,602,946-99,606,130 , GRCh37.p13 chr6: 100,050,822-100,054,006 PRDM13
    nsv6805379copy number variation1nstd229human GRCh38 chr6: 99,603,901-99,612,000 , GRCh37.p13 chr6: 100,051,777-100,059,876 PRDM13
    nsv6798292copy number variation1nstd229human GRCh38 chr6: 99,603,370-99,605,274 , GRCh37.p13 chr6: 100,051,246-100,053,150 PRDM13
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6608127copy number variation1nstd223human GRCh38 chr6: 99,606,413-99,627,797 , GRCh37.p13 chr6: 100,054,289-100,075,673 PRDM13
    nsv6607067copy number variation1nstd223human GRCh38 chr6: 99,588,501-99,620,600 , GRCh37.p13 chr6: 100,036,377-100,068,476 PRDM13
    nsv6314491complex chromosomal rearrangement13nstd102humanUncertain significance GRCh37 chr3: 79,816,988-79,816,988 , GRCh37 chr3: 79,973,297-79,973,297 , GRCh37 chr3: 79,973,300-79,973,300 , GRCh37 chr3: 81,581,577-81,581,577 , GRCh37 chr6: 100,444,315-100,444,315 , GRCh37 chr12: 43,746,118-43,746,118 , GRCh37 chr2: 161,894,555-161,894,555 , GRCh37 chr2: 161,894,562-161,894,562 , GRCh37 chr2: 161,991,423-161,991,423 , GRCh37 chr2: 161,991,426-161,991,426 , GRCh37 chr6: 100,056,300-100,056,300 , GRCh37 chr6: 100,241,597-100,241,597 , GRCh37 chr6: 100,444,952-100,444,952 , GRCh37 chr6: 100,444,952-100,444,952 , GRCh37 chr3: 81,581,572-81,581,572 , GRCh37 chr6: 128,199,157-128,199,157 , GRCh37 chr21: 16,441,449-16,441,449 , GRCh37 chr21: 16,441,585-16,441,585 , GRCh37 chr3: 79,817,414-79,817,414 , GRCh37 chr6: 100,056,301-100,056,301 , GRCh37 chr6: 100,241,586-100,241,586 , GRCh37 chr6: 100,444,299-100,444,299 , GRCh37 chr6: 128,199,163-128,199,163 , GRCh37 chr12: 43,450,556-43,450,556 , GRCh37 chr12: 43,450,581-43,450,581 , GRCh37 chr12: 43,746,119-43,746,119 , GRCh38.p12 chr12: 43,056,753-43,056,753 , GRCh38.p12 chr12: 43,352,316-43,352,316 , GRCh38.p12 chr21: 15,069,128-15,069,128 , GRCh38.p12 chr3: 79,767,838-79,767,838 , GRCh38.p12 chr6: 127,878,012-127,878,012 , GRCh38.p12 chr12: 43,056,778-43,056,778 , GRCh38.p12 chr2: 161,038,044-161,038,044 , GRCh38.p12 chr2: 161,134,912-161,134,912 , GRCh38.p12 chr21: 15,069,264-15,069,264 , GRCh38.p12 chr6: 99,608,424-99,608,424 , GRCh38.p12 chr6: 99,793,721-99,793,721 , GRCh38.p12 chr6|NT_187556.1: 223,210-223,210 , GRCh38.p12 chr3: 79,768,264-79,768,264 , GRCh38.p12 chr3: 79,924,150-79,924,150 , GRCh38.p12 chr3: 81,532,426-81,532,426 , GRCh38.p12 chr6: 99,996,423-99,996,423 , GRCh38.p12 chr6: 99,996,439-99,996,439 , GRCh38.p12 chr12: 43,352,315-43,352,315 , GRCh38.p12 chr2: 161,038,051-161,038,051 , GRCh38.p12 chr2: 161,134,915-161,134,915 , GRCh38.p12 chr3: 79,924,147-79,924,147 , GRCh38.p12 chr3: 81,532,421-81,532,421 , GRCh38.p12 chr6: 99,608,425-99,608,425 , GRCh38.p12 chr6: 99,793,710-99,793,710 , GRCh38.p12 chr6: 99,997,076-99,997,076 , GRCh38.p12 chr6: 99,997,076-99,997,076 , GRCh38.p12 chr6: 127,878,018-127,878,018 , GRCh38.p12 chr6|NT_187556.1: 223,216-223,216 GBE1, ROBO1, 5 more genes
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv5564351copy number variation1nstd102humanUncertain significance GRCh37 chr6: 100,054,911-100,062,635 , GRCh38.p12 chr6: 99,607,035-99,614,759 PRDM13
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4683491copy number variation1nstd102humanUncertain significance GRCh37 chr6: 99,997,384-100,062,635 , GRCh38.p12 chr6: 99,549,508-99,614,759 RPS3P5, PRDM13, 2 more genes
    nsv4683054copy number variation1nstd102humanUncertain significance GRCh37 chr6: 100,010,718-100,062,635 , GRCh38.p12 chr6: 99,562,842-99,614,759 PRDM13, RPS3P5, 2 more genes
    nsv4675136copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 98,870,687-100,270,433 , GRCh38.p12 chr6: 98,422,811-99,822,557 CCNC, POU3F2, 13 more genes
    nsv4457050copy number variation1nstd102humanUncertain significance GRCh37 chr6: 99,158,119-100,269,911 , GRCh38.p12 chr6: 98,710,243-99,822,035 TSTD3, BDH2P1, 12 more genes
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