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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6803850copy number variation1nstd229human GRCh38 chr6: 99,868,143-100,064,208 , GRCh37.p13 chr6: 100,316,019-100,512,084 MCHR2-AS1, MCHR2, 1 more genes
    nsv6636908copy number variation1nstd102humanUncertain significance GRCh37 chr6: 100,403,323-100,774,188 , GRCh38.p12 chr6: 99,955,447-100,326,312 MCHR2-AS1, PRDX2P4, 5 more genes
    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
    nsv6630468copy number variation1nstd224human GRCh37 chr6: 100,277,840-100,642,867 , GRCh38.p12 chr6: 99,829,964-100,194,991 MCHR2, PRDX2P4, 5 more genes
    nsv6610948copy number variation1nstd223human GRCh38 chr6: 99,837,134-100,086,836 , GRCh37.p13 chr6: 100,285,010-100,534,712 NPM1P38, MCHR2-AS1, 1 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
    nsv5473745copy number variation1nstd206human GRCh38 chr6: 100,041,686-100,088,796 , GRCh37.p13 chr6: 100,489,562-100,536,672 NPM1P38, MCHR2-AS1
    nsv5222913copy number variation1nstd204human GRCh37.p13 chr6: 100,274,277-100,645,576 , GRCh38.p13 chr6: 99,826,401-100,197,700 MCHR2, PRDX2P4, 5 more genes
    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
    nsv4680166copy number variation1nstd189human GRCh37.p13 chr6: 100,270,087-100,690,918 , GRCh38.p12 chr6: 99,822,211-100,243,042 MCHR2, PRDX2P4, 5 more genes
    nsv4524119copy number variation1nstd166human GRCh37.p13 chr6: 100,276,998-100,645,000 , GRCh38.p12 chr6: 99,829,122-100,197,124 MCHR2, PRDX2P4, 5 more genes
    nsv4400054copy number variation1nstd174human GRCh37 chr6: 100,277,840-100,650,498 , GRCh38.p12 chr6: 99,829,964-100,202,622 MCHR2, PRDX2P4, 5 more genes
    nsv4378028copy number variation1nstd173human GRCh37 chr6: 100,269,911-100,643,678 , GRCh38.p12 chr6: 99,822,035-100,195,802 NPM1P38, LOC105377911, 5 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
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 TUBE1, PLN, 318 more genes
    nsv3922363copy number variation1nstd102humanUncertain significance NCBI36 chr6: 100,385,720-100,749,562 , GRCh37 chr6: 100,278,999-100,642,841 , GRCh38 chr6: 99,831,123-100,194,965 MCHR2-AS1, LOC100129854, 5 more genes
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