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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
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6799136copy number variation1nstd229human GRCh38 chr6: 110,326,547-111,405,944 , GRCh37.p13 chr6: 110,647,750-111,727,147 RPS19P5, REV3L, 30 more genes
    nsv6603104copy number variation1nstd223human GRCh38 chr6: 110,597,001-110,599,400 , GRCh37.p13 chr6: 110,918,204-110,920,603 LOC100420531
    nsv6567864inversion1nstd223human GRCh38 chr6: 109,778,846-111,235,585 , GRCh37.p13 chr6: 110,100,049-111,556,788 RNU6-1115P, GSTM2P1, 33 more genes
    nsv6315400copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,713,707-111,100,242 , GRCh38.p12 chr6: 110,392,504-110,779,039 RPS19P5, SLC22A16, 12 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
    nsv6313613copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,472,732-114,762,836 , GRCh38.p12 chr6: 110,151,529-114,441,672 LOC107986522, TUBE1, 87 more genes
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942835copy number variation1nstd200human GRCh38 chr6: 110,597,634-110,597,713 , GRCh37.p13 chr6: 110,918,837-110,918,916 LOC100420531
    nsv4942834copy number variation1nstd200human GRCh38 chr6: 110,595,735-110,598,316 , GRCh37.p13 chr6: 110,916,938-110,919,519 LOC100420531
    nsv4817520copy number variation1nstd200human GRCh37 chr6: 110,916,938-110,919,519 , GRCh38.p12 chr6: 110,595,735-110,598,316 LOC100420531
    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
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4674911copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,564,694-112,232,351 , GRCh38.p12 chr6: 109,243,491-111,911,148 LOC105377939, LOC105377945, 57 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4312499inversion1nstd166human GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456 , CRYBG1, 284 more genes
    nsv3962635insertion1nstd168human GRCh38 chr6: 110,581,502-110,614,371 , GRCh37.p13 chr6: 110,902,705-110,935,574 CDK19, LOC100420531, 1 more genes
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