U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 963

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv5596copy number variation1estd19human NCBI36 chr18: 98,196-98,424 , GRCh37.p13 chr18: 108,196-108,424 , GRCh38.p12 chr18: 108,196-108,424 ROCK1P1
    esv8645copy number variation1estd19human NCBI36 chr10: 89,884,247-89,884,474 , GRCh37.p13 chr10: 89,894,267-89,894,494 , GRCh38.p12 chr10: 88,134,510-88,134,737 LOC101929727
    esv7139copy number variation1estd19human NCBI36 chr20: 59,337,787-59,338,013 , GRCh37.p13 chr20: 59,904,392-59,904,618 , GRCh38.p12 chr20: 61,329,336-61,329,562 CDH4
    esv8308copy number variation1estd19human NCBI36 chr4: 110,141,877-110,142,102 , GRCh37.p13 chr4: 109,922,428-109,922,653 , GRCh38.p12 chr4: 109,001,272-109,001,497 COL25A1
    esv6946copy number variation1estd19human NCBI36 chr4: 10,309,917-10,310,139 , GRCh37.p13 chr4: 10,700,819-10,701,041 , GRCh38.p12 chr4: 10,699,195-10,699,417 CLNK
    esv8521copy number variation1estd19human NCBI36 chr10: 113,660,157-113,660,378 , GRCh37.p13 chr10: 113,670,167-113,670,388 , GRCh38.p12 chr10: 111,910,409-111,910,630
    esv6206copy number variation1estd19human NCBI36 chr18: 99,282-99,503 , GRCh37.p13 chr18: 109,282-109,503 , GRCh38.p12 chr18: 109,282-109,503 ROCK1P1
    esv7535copy number variation1estd19human NCBI36 chr2: 37,642,546-37,642,766 , GRCh37.p13 chr2: 37,789,042-37,789,262 , GRCh38.p12 chr2: 37,561,899-37,562,119 LINC03063
    esv5515copy number variation1estd19human NCBI36 chr2: 132,750,904-132,751,123 , GRCh37.p13 chr2: 133,034,434-133,034,653 , GRCh38.p12 chr2: 132,276,861-132,277,080 LOC105373622
    esv7863copy number variation1estd19human NCBI36 chr9: 85,025,012-85,025,230 , GRCh37.p13 chr9: 85,835,192-85,835,410 , GRCh38.p12 chr9: 83,220,277-83,220,495 FRMD3-AS1
    esv6168copy number variation1estd19human NCBI36 chr7: 36,927,136-36,927,354 , GRCh37.p13 chr7: 36,960,611-36,960,829 , GRCh38.p12 chr7: 36,921,006-36,921,224 ELMO1
    esv5759copy number variation1estd19human NCBI36 chr7: 157,896,348-157,896,565 , GRCh37.p13 chr7: 158,203,587-158,203,804 , GRCh38.p12 chr7: 158,410,895-158,411,112 , GRCh38.p12 chr7|NT_187560.1: 66,063-66,280 PTPRN2
    esv9313copy number variation1estd19human NCBI36 chr21: 16,858,796-16,859,012 , GRCh37.p13 chr21: 17,936,925-17,937,141 , GRCh38.p12 chr21: 16,564,605-16,564,821 MIR99AHG
    esv8395copy number variation1estd19human NCBI36 chr5: 19,690,103-19,690,319 , GRCh37.p13 chr5: 19,654,346-19,654,562 , GRCh38.p12 chr5: 19,654,237-19,654,453 CDH18
    esv7545copy number variation1estd19human NCBI36 chr7: 157,896,186-157,896,402 , GRCh37.p13 chr7: 158,203,425-158,203,641 , GRCh38.p12 chr7: 158,410,733-158,410,949 , GRCh38.p12 chr7|NT_187560.1: 66,226-66,442 PTPRN2
    esv9030copy number variation1estd19human NCBI36 chr6: 158,603,885-158,604,100 , GRCh37.p13 chr6: 158,683,897-158,684,112 , GRCh38.p12 chr6: 158,262,865-158,263,080 TULP4
    esv8271copy number variation1estd19human NCBI36 chr10: 33,424,371-33,424,586 , GRCh37.p13 chr10: 33,384,365-33,384,580 , GRCh38.p12 chr10: 33,095,437-33,095,652 IATPR
    esv7090copy number variation1estd19human NCBI36 chr13: 112,347,535-112,347,750 , GRCh37.p13 chr13: 113,299,534-113,299,749 , GRCh38.p12 chr13: 112,645,220-112,645,435 ATP11AUN
    esv7009copy number variation1estd19human NCBI36 chr1: 239,844,642-239,844,857 , GRCh37.p13 chr1: 241,778,019-241,778,234 , GRCh38.p12 chr1: 241,614,717-241,614,932 OPN3
    esv6412copy number variation1estd19human NCBI36 chr7: 84,047,643-84,047,858 , GRCh37.p13 chr7: 84,209,707-84,209,922 , GRCh38.p12 chr7: 84,580,391-84,580,606 LINC03017
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center