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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137802copy number variation1nstd232human GRCh37.p13 chr8: 145,005,448-145,005,560 , GRCh38.p12 chr8: 143,931,280-143,931,392 PLEC
    nsv7097788copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,047,551-145,049,537 , GRCh38.p12 chr8: 143,973,383-143,975,369 PLEC, PARP10
    nsv6873776copy number variation1nstd229human GRCh38 chr8: 143,662,901-144,626,400 , GRCh37.p13 chr8: 145,146,063-145,851,785 LRRC14, SCX, 67 more genes
    nsv6873663copy number variation1nstd229human GRCh38 chr8: 143,923,401-143,925,800 , GRCh37.p13 chr8|NW_003315923.1: 262,046-264,445 , GRCh37.p13 chr8: 144,997,569-144,999,968 PLEC
    nsv6872984copy number variation1nstd229human GRCh38 chr8: 143,875,801-143,973,300 , GRCh37.p13 chr8|NW_003315923.1: 214,446-311,945 , GRCh37.p13 chr8: 144,949,969-145,047,468 MIR661, PLEC, 1 more genes
    nsv6871595copy number variation1nstd229human GRCh38 chr8: 143,922,901-143,925,000 , GRCh37.p13 chr8|NW_003315923.1: 261,546-263,645 , GRCh37.p13 chr8: 144,997,069-144,999,168 PLEC
    nsv6870623copy number variation1nstd229human GRCh38 chr8: 143,963,567-143,969,238 , GRCh37.p13 chr8|NW_003315923.1: 302,212-307,883 , GRCh37.p13 chr8: 145,037,735-145,043,406 PLEC
    nsv6868488copy number variation1nstd229human GRCh38 chr8: 143,952,325-143,952,455 , GRCh37.p13 chr8|NW_003315923.1: 290,970-291,100 , GRCh37.p13 chr8: 145,026,493-145,026,623 PLEC
    nsv6866250copy number variation1nstd229human GRCh38 chr8: 143,771,901-144,562,100 , GRCh37.p13 chr8: 145,146,063-145,787,484 MIR939, MIR10400, 58 more genes
    nsv6864443copy number variation1nstd229human GRCh38 chr8: 143,909,126-143,915,037 , GRCh37.p13 chr8: 144,983,294-144,989,205 , GRCh37.p13 chr8|NW_003315923.1: 247,771-253,682 PLEC
    nsv6864240copy number variation1nstd229human GRCh38 chr8: 143,925,501-143,931,300 , GRCh37.p13 chr8: 144,999,669-145,005,468 , GRCh37.p13 chr8|NW_003315923.1: 264,146-269,945 PLEC
    nsv6863313copy number variation1nstd229human GRCh38 chr8: 143,829,301-143,950,800 , GRCh37.p13 chr8|NW_003315923.1: 167,946-289,445 , GRCh37.p13 chr8: 144,911,471-145,024,968 PLEC, EPPK1, 5 more genes
    nsv6863270copy number variation1nstd229human GRCh38 chr8: 143,924,101-143,925,600 , GRCh37.p13 chr8|NW_003315923.1: 262,746-264,245 , GRCh37.p13 chr8: 144,998,269-144,999,768 PLEC
    nsv6861967copy number variation1nstd229human GRCh38 chr8: 143,942,330-143,942,403 , GRCh37.p13 chr8: 145,016,498-145,016,571 , GRCh37.p13 chr8|NW_003315923.1: 280,975-281,048 PLEC
    nsv6861795copy number variation1nstd229human GRCh38 chr8: 143,924,701-143,929,900 , GRCh37.p13 chr8: 144,998,869-145,004,068 , GRCh37.p13 chr8|NW_003315923.1: 263,346-268,545 PLEC
    nsv6859198copy number variation1nstd229human GRCh38 chr8: 143,837,839-143,924,644 , GRCh37.p13 chr8: 144,920,011-144,998,812 , GRCh37.p13 chr8|NW_003315923.1: 176,484-263,289 EPPK1, PLEC, 2 more genes
    nsv6858826copy number variation1nstd229human GRCh38 chr8: 143,883,317-143,940,963 , GRCh37.p13 chr8|NW_003315923.1: 221,962-279,608 , GRCh37.p13 chr8: 144,957,485-145,015,131 PLEC
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632761copy number variation1nstd224human GRCh37 chr8: 144,944,735-144,991,208 , GRCh38.p12 chr8: 143,870,567-143,917,040 PLEC, EPPK1
    nsv6632760copy number variation2nstd224human GRCh37 chr8: 144,943,389-145,003,862 , GRCh38.p12 chr8: 143,869,221-143,929,694 PLEC, EPPK1
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