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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097560copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 107,019,871-110,266,416 , GRCh38.p12 chr6: 106,571,996-109,945,213 ZPR1P1, OSTM1, 60 more genes
    nsv6814673copy number variation1nstd229human GRCh38 chr6: 106,804,490-107,038,337 , GRCh37.p13 chr6|NW_004504300.1: 109,113-342,960 MTRES1, HMGN2P12, 3 more genes
    nsv6811595copy number variation1nstd229human GRCh38 chr6: 106,944,101-107,248,300 , GRCh37.p13 chr6|NW_004504300.1: 248,724-478,993 , GRCh37.p13 chr6: 107,309,895-107,495,574 CD24, BEND3, 5 more genes
    nsv6807684copy number variation1nstd229human GRCh38 chr6: 106,848,361-106,974,629 , GRCh37.p13 chr6|NW_004504300.1: 152,984-279,252 HMGN2P12, CD24, 2 more genes
    nsv6804847copy number variation1nstd229human GRCh38 chr6: 105,481,597-109,225,980 , GRCh37.p13 chr6: 105,929,472-109,547,183 LINC02836, SOBP, 61 more genes
    nsv6636537copy number variation1nstd102humanUncertain significance GRCh37 chr6: 107,302,955-107,443,197 , GRCh38.p12 chr6: 106,855,080-107,121,993 HMGN2P12, MTRES1, 4 more genes
    nsv6613052copy number variation1nstd223human GRCh38 chr6: 106,848,352-106,974,652 , GRCh37.p13 chr6|NW_004504300.1: 152,975-279,275 LOC107986534, CD24, 2 more genes
    nsv6607176copy number variation1nstd223human GRCh38 chr6: 106,976,236-106,976,944 , GRCh37.p13 chr6|NW_004504300.1: 280,859-281,567 CD24
    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
    nsv6136157copy number variation1nstd213human GRCh37 chr6: 106,730,000-107,440,001 , GRCh38.p12 chr6: 106,282,125-107,118,797 CRYBG1, HMGN2P12, 20 more genes
    nsv5381620copy number variation1nstd102humanUncertain significance GRCh37 chr6: 106,756,239-107,365,536 , GRCh38.p12 chr6: 106,308,364-107,044,332 CRYBG1, RPL21P65, 17 more genes
    nsv5233995copy number variation1nstd204human GRCh38.p13 chr6: 106,969,901-106,971,600 , GRCh37.p13 chr6|NW_004504300.1: 274,524-276,223 CD24
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945516copy number variation1nstd200human GRCh38 chr6: 106,848,361-106,974,631 , GRCh37.p13 chr6|NW_004504300.1: 152,984-279,254 HMGN2P12, LOC105377928, 2 more genes
    nsv4942735copy number variation1nstd200human GRCh38 chr6: 106,968,997-106,969,120 , GRCh37.p13 chr6|NW_004504300.1: 273,620-273,743 CD24
    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
    nsv4675563copy number variation1nstd102humanUncertain significance GRCh37 chr6: 106,638,006-107,421,916 , GRCh38.p12 chr6: 106,190,131-107,100,712 QRSL1, ATG5, 20 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
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