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Items: 15

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    Number of Variants: 15

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3598186copy number variation5estd214human GRCh37 (hg19) chr3: 151,463,357-151,475,947 , GRCh38 (hg38) chr3|NW_003315913.1: 166,742-179,332 , GRCh38 (hg38) chr3: 151,745,569-151,758,159 AADACL2-AS1, AADACL2
    esv3598181copy number variation1estd214human GRCh37 (hg19) chr3: 151,323,737-151,330,161 , GRCh38 (hg38) chr3|NW_003315913.1: 16,584-23,008 , GRCh38 (hg38) chr3: 151,605,949-151,612,373 IGSF10
    esv3598179copy number variation1estd214human GRCh37 (hg19) chr3: 151,311,578-151,412,954 , GRCh38 (hg38) chr3: 151,593,790-151,695,166 , GRCh38 (hg38) chr3|NW_003315913.1: 4,425-116,339 IGSF10
    esv3598178copy number variation1estd214human GRCh37 (hg19) chr3: 151,311,566-151,371,388 , GRCh38 (hg38) chr3|NW_003315913.1: 4,413-64,228 , GRCh38 (hg38) chr3: 151,593,778-151,653,600 IGSF10
    esv3598183copy number variation2estd214human GRCh37 (hg19) chr3: 151,395,580-151,419,127 , GRCh38 (hg38) chr3|NW_003315913.1: 98,965-122,512 , GRCh38 (hg38) chr3: 151,677,792-151,701,339 0
    esv3598182copy number variation1estd214human GRCh37 (hg19) chr3: 151,383,442-151,394,390 , GRCh38 (hg38) chr3|NW_003315913.1: 86,813-97,775 , GRCh38 (hg38) chr3: 151,665,654-151,676,602 0
    esv3598185copy number variation1estd214human GRCh37 (hg19) chr3: 151,418,344-151,432,121 , GRCh38 (hg38) chr3: 151,700,556-151,714,333 , GRCh38 (hg38) chr3|NW_003315913.1: 121,729-135,506 0
    esv3598177mobile element insertion12estd214human GRCh37 (hg19) chr3: 151,309,018-151,309,018 , GRCh38 (hg38) chr3: 151,591,230-151,591,230 , GRCh38 (hg38) chr3|NW_003315913.1: 1,865-1,865 IGSF10
    esv3598180mobile element insertion3estd214human GRCh37 (hg19) chr3: 151,316,156-151,316,156 , GRCh38 (hg38) chr3|NW_003315913.1: 9,003-9,003 , GRCh38 (hg38) chr3: 151,598,368-151,598,368 IGSF10
    esv3447328copy number variation1estd59human NCBI36 (hg18) chr3: 152,951,677-152,952,049 , GRCh37.p13 chr3|NW_003315913.1: 172,372-172,744 , GRCh37 (hg19) chr3: 151,468,987-151,469,359 , GRCh38 (hg38) chr3|NW_003315913.1: 172,372-172,744 , GRCh38 (hg38) chr3: 151,751,199-151,751,571 AADACL2-AS1, AADACL2
    esv3449164copy number variation1estd59human NCBI36 (hg18) chr3: 152,907,993-152,936,129 , GRCh37 (hg19) chr3: 151,425,303-151,453,439 , GRCh37.p13 chr3|NW_003315913.1: 128,688-156,824 , GRCh38 (hg38) chr3: 151,707,515-151,735,651 , GRCh38 (hg38) chr3|NW_003315913.1: 128,688-156,824 AADACL2
    esv3388197copy number variation1estd59human NCBI36 (hg18) chr3: 152,908,097-152,908,417 , GRCh37.p13 chr3|NW_003315913.1: 128,792-129,112 , GRCh37 (hg19) chr3: 151,425,407-151,425,727 , GRCh38 (hg38) chr3|NW_003315913.1: 128,792-129,112 , GRCh38 (hg38) chr3: 151,707,619-151,707,939 0
    esv3386691insertion1estd59human NCBI36 (hg18) chr3: 152,933,006-152,933,191 , GRCh37.p13 chr3|NW_003315913.1: 153,701-153,886 , GRCh37 (hg19) chr3: 151,450,316-151,450,501 , GRCh38 (hg38) chr3: 151,732,528-151,732,713 , GRCh38 (hg38) chr3|NW_003315913.1: 153,701-153,886 0
    esv3330051copy number variation2estd59human NCBI36 (hg18) chr3: 152,931,752-152,933,900 , GRCh37.p13 chr3|NW_003315913.1: 152,447-154,595 , GRCh37 (hg19) chr3: 151,449,062-151,451,210 , GRCh38 (hg38) chr3: 151,731,274-151,733,422 , GRCh38 (hg38) chr3|NW_003315913.1: 152,447-154,595 0
    nsv480864novel sequence insertion1nstd35human GRCh37.p13 chr3|NW_003315913.1: 78,567-80,329 , GRCh38 (hg38) chr3|NW_003315913.1: 78,567-80,329 , GRCh38.p2 chr3|NW_001838884.2: 42,662,274-42,664,036 0
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