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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6711851copy number variation1nstd229human GRCh38 chr3: 49,126,501-49,128,455 , GRCh37.p13 chr3: 49,163,934-49,165,888 LAMB2
    nsv1127958copy number variation1nstd106human GRCh37 chr3: 49,164,890-49,164,955 , GRCh38.p12 chr3: 49,127,457-49,127,522 LAMB2
    esv3440944copy number variation8estd59human NCBI36 chr3: 49,136,502-49,139,300 , GRCh37.p13 chr3: 49,161,498-49,164,296 , GRCh38.p12 chr3: 49,124,065-49,126,863 LAMB2
    esv1585419copy number variation1estd22human NCBI36 chr3: 49,134,913-49,134,914 , GRCh37.p13 chr3: 49,159,909-49,159,910 , GRCh38.p12 chr3: 49,122,476-49,122,477 LAMB2
    nsv5435229copy number variation1nstd206human GRCh38 chr3: 49,127,486-49,127,811 , GRCh37.p13 chr3: 49,164,919-49,165,244 LAMB2
    nsv4914309copy number variation1nstd200human GRCh38 chr3: 49,121,824-49,122,886 , GRCh37.p13 chr3: 49,159,257-49,160,319 LAMB2
    nsv4793981copy number variation1nstd200human GRCh37 chr3: 49,159,257-49,160,319 , GRCh38.p12 chr3: 49,121,824-49,122,886 LAMB2
    nsv3129961copy number variation1nstd151human GRCh37 chr3: 49,159,374-49,162,922 , GRCh38.p12 chr3: 49,121,941-49,125,489 LAMB2
    nsv3131763copy number variation1nstd151human GRCh37 chr3: 49,159,114-49,162,607 , GRCh38.p12 chr3: 49,121,681-49,125,174 LAMB2
    esv3340652copy number variation1estd59human NCBI36 chr3: 49,141,952-49,145,750 , GRCh37.p13 chr3: 49,166,948-49,170,746 , GRCh38.p12 chr3: 49,129,515-49,133,313 LAMB2
    nsv7050004inversion1nstd229human GRCh38 chr3: 49,123,013-49,123,177 , GRCh37.p13 chr3: 49,160,446-49,160,610 LAMB2
    nsv2167617short tandem repeat1nstd128human GRCh37 chr3: 49,164,414-49,164,437 , GRCh38.p12 chr3: 49,126,981-49,127,004 LAMB2
    nsv2170845short tandem repeat1nstd128human GRCh37 chr3: 49,165,130-49,165,152 , GRCh38.p12 chr3: 49,127,697-49,127,719 LAMB2
    nsv6710139copy number variation1nstd229human GRCh38 chr3: 49,119,282-49,120,754 , GRCh37.p13 chr3: 49,156,715-49,158,187 LAMB2, USP19
    nsv3130992copy number variation3nstd151human GRCh37 chr3: 49,158,656-49,162,922 , GRCh38.p12 chr3: 49,121,223-49,125,489 LAMB2, USP19
    nsv3136481copy number variation1nstd151human GRCh37 chr3: 49,158,656-49,163,935 , GRCh38.p12 chr3: 49,121,223-49,126,502 LAMB2, USP19
    nsv3131040copy number variation1nstd151human GRCh37 chr3: 49,158,656-49,161,724 , GRCh38.p12 chr3: 49,121,223-49,124,291 LAMB2, USP19
    nsv3135962copy number variation1nstd151human GRCh37 chr3: 49,158,863-49,161,069 , GRCh38.p12 chr3: 49,121,430-49,123,636 USP19, LAMB2
    nsv3121408copy number variation1nstd151human GRCh37 chr3: 49,158,656-49,159,808 , GRCh38.p12 chr3: 49,121,223-49,122,375 USP19, LAMB2
    nsv3119025copy number variation1nstd151human GRCh37 chr3: 49,158,656-49,201,646 , GRCh38.p12 chr3: 49,121,223-49,164,213 LAMB2P1, LAMB2, 2 more genes
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