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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6639831copy number variation1nstd229human GRCh38 chr1: 110,514,701-110,531,300 , GRCh37.p13 chr1: 111,057,323-111,073,922 KCNA10
    esv2998130copy number variation1estd209human GRCh37 chr1: 111,059,812-111,059,814 , GRCh38.p12 chr1: 110,517,190-110,517,192 KCNA10
    nsv547498copy number variation1nstd54human NCBI36 chr1: 110,836,697-110,862,585 , GRCh37.p13 chr1: 111,035,174-111,061,062 , GRCh38.p12 chr1: 110,492,552-110,518,440 KCNA10
    nsv6639788copy number variation1nstd229human GRCh38 chr1: 110,513,001-110,518,716 , GRCh37.p13 chr1: 111,055,623-111,061,338 KCNA10
    nsv1455939short tandem repeat3nstd128human GRCh37 chr1: 111,059,790-111,059,844 , GRCh38.p12 chr1: 110,517,168-110,517,222 KCNA10
    nsv1458806short tandem repeat1nstd128human GRCh37 chr1: 111,058,334-111,058,358 , GRCh38.p12 chr1: 110,515,712-110,515,736 KCNA10
    nsv1455938short tandem repeat1nstd128human GRCh37 chr1: 111,058,286-111,058,298 , GRCh38.p12 chr1: 110,515,664-110,515,676 KCNA10
    nsv6639785copy number variation1nstd229human GRCh38 chr1: 110,476,163-110,601,124 , GRCh37.p13 chr1: 111,018,785-111,143,746 KCNA10, CYMP, 2 more genes
    nsv4579089copy number variation1nstd183human GRCh37 chr1: 111,019,774-111,144,955 , GRCh38.p12 chr1: 110,477,152-110,602,333 KCNA10, CYMP, 2 more genes
    nsv2743708copy number variation1nstd130human NCBI36 chr1: 110,823,251-110,943,205 , GRCh37.p13 chr1: 111,021,728-111,141,682 , GRCh38.p12 chr1: 110,479,106-110,599,060 KCNA10, KCNA2, 2 more genes
    nsv2748258copy number variation1nstd130human NCBI36 chr1: 110,823,251-110,941,683 , GRCh37.p13 chr1: 111,021,728-111,140,160 , GRCh38.p12 chr1: 110,479,106-110,597,538 KCNA10, CYMP-AS1, 2 more genes
    nsv1305111copy number variation1nstd122human NCBI36 chr1: 110,823,251-110,945,530 , GRCh37.p13 chr1: 111,021,728-111,144,007 , GRCh38.p12 chr1: 110,479,106-110,601,385 KCNA10, CYMP, 2 more genes
    nsv1313244copy number variation1nstd122human NCBI36 chr1: 110,823,998-110,946,184 , GRCh37.p13 chr1: 111,022,475-111,144,661 , GRCh38.p12 chr1: 110,479,853-110,602,039 KCNA10, KCNA2, 2 more genes
    nsv1006346copy number variation2nstd100human NCBI36 chr1: 110,821,297-110,944,668 , GRCh37.p13 chr1: 111,019,774-111,143,145 , GRCh38.p12 chr1: 110,477,152-110,600,523 KCNA10, CYMP, 2 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 KCNA10, LINC01307, 320 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 KCNA10, AMYP1, 320 more genes
    nsv3893941copy number variation1nstd102humanPathogenic NCBI36 chr1: 97,648,746-111,014,655 , GRCh37 chr1: 97,876,158-111,213,132 , GRCh38 chr1: 97,410,602-110,670,510 KCNA10, RPSAP19, 196 more genes
    nsv3901500copy number variation1nstd102humanPathogenic NCBI36 chr1: 101,856,241-112,047,173 , GRCh38 chr1: 101,618,097-111,703,028 , GRCh37 chr1: 102,083,653-112,245,650 KCNA10, CHIAP1, 171 more genes
    nsv3920130copy number variation1nstd102humanPathogenic NCBI36 chr1: 103,429,843-112,252,782 , GRCh37.p13 chr1: 103,657,255-112,451,259 , GRCh38.p12 chr1: 103,191,699-111,908,637 KCNA10, LOC105378898, 166 more genes
    nsv3901806copy number variation1nstd102humanPathogenic NCBI36 chr1: 105,812,437-112,534,771 , GRCh38 chr1: 105,468,292-112,190,626 , GRCh37 chr1: 106,010,914-112,733,248 KCNA10, LOC126987, 151 more genes
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