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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6811932copy number variation1nstd229human GRCh38 chr6: 89,752,786-89,913,243 , GRCh37.p13 chr6: 90,462,505-90,622,962 LOC644269, PIMREGP3, 5 more genes
    nsv6808775copy number variation1nstd229human GRCh38 chr6: 89,412,459-89,922,314 , GRCh37.p13 chr6: 90,122,178-90,632,033 RN7SL11P, LOC105377889, 12 more genes
    nsv6807153copy number variation1nstd229human GRCh38 chr6: 89,617,897-89,897,461 , GRCh37.p13 chr6: 90,327,616-90,607,180 LOC644269, GJA10, 8 more genes
    nsv6803990copy number variation1nstd229human GRCh38 chr6: 89,834,480-89,939,780 , GRCh37.p13 chr6: 90,544,199-90,649,499 BACH2, LOC644269, 3 more genes
    nsv6802932copy number variation1nstd229human GRCh38 chr6: 88,525,377-89,929,877 , GRCh37.p13 chr6: 89,235,096-90,639,596 GJA10, RN7SL11P, 27 more genes
    nsv6798946copy number variation1nstd229human GRCh38 chr6: 89,877,901-89,920,900 , GRCh37.p13 chr6: 90,587,620-90,630,619 GJA10, LOC644269
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6405432copy number variation1nstd223human GRCh38 chr6: 89,376,654-90,197,092 , GRCh37.p13 chr6: 90,086,373-90,906,811 MDN1, MDN1-AS1, 15 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6313743copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,189,085-90,697,359 , GRCh38.p12 chr6: 89,479,366-89,987,640 DNAJC19P6, MDN1, 10 more genes
    nsv6290854copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,008,961-93,761,490 , GRCh38.p12 chr6: 89,299,242-93,051,772 NACAP7, PIMREGP3, 38 more genes
    nsv6135855copy number variation1nstd213human GRCh37 chr6: 87,530,000-91,880,001 , GRCh38.p12 chr6: 86,820,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv6135527copy number variation1nstd213human GRCh37 chr6: 87,520,000-91,880,001 , GRCh38.p12 chr6: 86,810,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv5468890copy number variation1nstd206human GRCh38 chr6: 89,879,350-89,910,750 , GRCh37.p13 chr6: 90,589,069-90,620,469 LOC644269, GJA10
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942084copy number variation1nstd200human GRCh38 chr6: 89,877,911-89,920,895 , GRCh37.p13 chr6: 90,587,630-90,630,614 GJA10, LOC644269
    nsv4729396copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,285,430-90,706,261 , GRCh38.p12 chr6: 89,575,711-89,996,542 DNAJC19P6, MDN1, 9 more genes
    nsv4728930copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,085,893-90,910,484 , GRCh38.p12 chr6: 89,376,174-90,200,765 RRAGD, MDN1-AS1, 15 more genes
    nsv4675498copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,108,876-90,806,063 , GRCh38.p12 chr6: 89,399,157-90,096,344 RN7SL11P, LOC105377889, 14 more genes
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