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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144006insertion1nstd232human GRCh37.p13 chr5: 157,214,999-157,214,999 , GRCh38.p12 chr5: 157,787,991-157,787,991 CLINT1
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7055491inversion1nstd229human GRCh38 chr5: 157,701,805-157,831,931 , GRCh37.p13 chr5: 157,128,813-157,258,939 RNU6-260P, THG1L, 3 more genes
    nsv7052590inversion1nstd229human GRCh38 chr5: 154,695,187-159,271,728 , GRCh37.p13 chr5: 154,074,747-158,698,736 MRPL22, LOC105377673, 58 more genes
    nsv7043787inversion1nstd229human GRCh38 chr5: 157,840,676-157,840,702 , GRCh37.p13 chr5: 157,267,684-157,267,710 CLINT1
    nsv6797525copy number variation1nstd229human GRCh38 chr5: 157,824,101-157,835,000 , GRCh37.p13 chr5: 157,251,109-157,262,008 CLINT1
    nsv6797098copy number variation1nstd229human GRCh38 chr5: 157,835,001-157,839,300 , GRCh37.p13 chr5: 157,262,009-157,266,308 CLINT1
    nsv6794009copy number variation1nstd229human GRCh38 chr5: 157,837,995-157,842,534 , GRCh37.p13 chr5: 157,265,003-157,269,542 CLINT1
    nsv6789342copy number variation1nstd229human GRCh38 chr5: 157,841,377-157,841,427 , GRCh37.p13 chr5: 157,268,385-157,268,435 CLINT1
    nsv6783812copy number variation1nstd229human GRCh38 chr5: 157,851,431-157,855,206 , GRCh37.p13 chr5: 157,278,439-157,282,214 CLINT1
    nsv6780756copy number variation1nstd229human GRCh38 chr5: 157,796,974-157,797,247 , GRCh37.p13 chr5: 157,223,982-157,224,255 CLINT1
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6573463inversion1nstd223human GRCh38 chr5: 157,801,518-157,802,083 , GRCh37.p13 chr5: 157,228,526-157,229,091 CLINT1
    nsv6566110inversion1nstd223human GRCh38 chr5: 157,832,002-157,833,847 , GRCh37.p13 chr5: 157,259,010-157,260,855 CLINT1
    nsv6562219inversion1nstd223human GRCh38 chr5: 157,838,190-157,839,170 , GRCh37.p13 chr5: 157,265,198-157,266,178 CLINT1
    nsv6559560inversion1nstd223human GRCh38 chr5: 157,790,050-157,791,152 , GRCh37.p13 chr5: 157,217,058-157,218,160 CLINT1
    nsv6558888inversion1nstd223human GRCh38 chr5: 157,828,928-157,829,692 , GRCh37.p13 chr5: 157,255,936-157,256,700 CLINT1
    nsv6557238inversion1nstd223human GRCh38 chr5: 157,845,078-157,845,732 , GRCh37.p13 chr5: 157,272,086-157,272,740 CLINT1
    nsv6555710inversion1nstd223human GRCh38 chr5: 157,838,004-157,839,138 , GRCh37.p13 chr5: 157,265,012-157,266,146 CLINT1
    nsv6413567copy number variation1nstd223human GRCh38 chr5: 157,807,901-157,810,200 , GRCh37.p13 chr5: 157,234,909-157,237,208 RNU6-260P, CLINT1
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