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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7097328copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,155,839-3,226,065 , GRCh38.p12 chr6: 3,155,605-3,225,831 TUBB2A, TUBB2BP1, 3 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7048211inversion1nstd229human GRCh38 chr6: 3,196,000-3,200,815 , GRCh37.p13 chr6: 3,196,234-3,201,049 LINC02525
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7044205inversion1nstd229human GRCh38 chr6: 2,472,898-4,774,625 , GRCh37.p13 chr6: 2,473,132-4,774,859 TOMM5P1, PXDC1, 56 more genes
    nsv6790680copy number variation1nstd229human GRCh38 chr6: 3,193,715-3,196,236 , GRCh37.p13 chr6: 3,193,949-3,196,470 LINC02525
    nsv6786779copy number variation1nstd229human GRCh38 chr6: 3,195,159-3,195,721 , GRCh37.p13 chr6: 3,195,393-3,195,955 LINC02525
    nsv6785298copy number variation1nstd229human GRCh38 chr6: 2,759,301-4,105,800 , GRCh37.p13 chr6: 2,759,535-4,106,034 LOC107986557, SERPINB9-AS1, 39 more genes
    nsv6781587copy number variation1nstd229human GRCh38 chr6: 3,185,087-3,190,708 , GRCh37.p13 chr6: 3,185,321-3,190,942 LINC02525
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6631163copy number variation1nstd224human GRCh37 chr6: 3,174,947-3,211,787 , GRCh38.p12 chr6: 3,174,713-3,211,553 LINC02525, TUBB2BP1
    nsv6631043copy number variation1nstd224human GRCh37 chr6: 3,162,378-3,211,787 , GRCh38.p12 chr6: 3,162,144-3,211,553 LINC02525, TUBB2BP1
    nsv6631042copy number variation1nstd224human GRCh37 chr6: 3,152,405-3,224,205 , GRCh38.p12 chr6: 3,152,171-3,223,971 BPHL, TUBB2A, 4 more genes
    nsv6574020inversion1nstd223human GRCh38 chr6: 3,192,446-3,192,989 , GRCh37.p13 chr6: 3,192,680-3,193,223 LINC02525
    nsv6414055copy number variation1nstd223human GRCh38 chr6: 3,195,159-3,195,720 , GRCh37.p13 chr6: 3,195,393-3,195,954 LINC02525
    nsv6404087copy number variation1nstd223human GRCh38 chr6: 3,181,801-3,182,300 , GRCh37.p13 chr6: 3,182,035-3,182,534 LINC02525
    nsv6314746copy number variation1nstd102humanPathogenic GRCh37 chr6: 375,263-3,655,142 , GRCh38.p12 chr6: 375,263-3,654,908 RN7SL352P, SERPINB8P1, 55 more genes
    nsv6313679copy number variation1nstd102humanPathogenic GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385 SERPINB9P1, LOC101927691, 59 more genes
    nsv6312036copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,154,097-3,226,065 , GRCh38.p12 chr6: 3,153,863-3,225,831 LINC02525, TUBB2BP1, 4 more genes
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