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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138960insertion1nstd232human GRCh37.p13 chr1: 93,620,450-93,620,450 , GRCh38.p12 chr1: 93,154,893-93,154,893 TMED5
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7054598inversion1nstd229human GRCh38 chr1: 92,942,106-93,208,617 , GRCh37.p13 chr1: 93,407,663-93,674,174 CCDC18, RNU6-970P, 7 more genes
    nsv7051334inversion1nstd229human GRCh38 chr1: 93,085,960-93,303,582 , GRCh37.p13 chr1: 93,551,517-93,769,139 MTF2, CCDC18, 4 more genes
    nsv6657362copy number variation1nstd229human GRCh38 chr1: 93,159,747-93,165,561 , GRCh37.p13 chr1: 93,625,304-93,631,118 TMED5
    nsv6657211copy number variation1nstd229human GRCh38 chr1: 93,177,615-93,177,650 , GRCh37.p13 chr1: 93,643,172-93,643,207 TMED5
    nsv6656648copy number variation1nstd229human GRCh38 chr1: 93,163,601-93,171,500 , GRCh37.p13 chr1: 93,629,158-93,637,057 TMED5
    nsv6656647copy number variation1nstd229human GRCh38 chr1: 93,144,210-93,150,126 , GRCh37.p13 chr1: 93,609,767-93,615,683 TMED5
    nsv6551293inversion1nstd223human GRCh38 chr1: 93,163,523-93,163,972 , GRCh37.p13 chr1: 93,629,080-93,629,529 TMED5
    nsv6543890inversion1nstd223human GRCh38 chr1: 93,157,892-93,158,616 , GRCh37.p13 chr1: 93,623,449-93,624,173 TMED5
    nsv6334688copy number variation1nstd223human GRCh38 chr1: 93,162,101-93,183,400 , GRCh37.p13 chr1: 93,627,658-93,648,957 TMED5, CCDC18
    nsv6329741copy number variation1nstd223human GRCh38 chr1: 93,153,101-93,154,600 , GRCh37.p13 chr1: 93,618,658-93,620,157 TMED5
    nsv6326539copy number variation1nstd223human GRCh38 chr1: 93,151,245-93,151,834 , GRCh37.p13 chr1: 93,616,802-93,617,391 TMED5
    nsv6320336copy number variation1nstd223human GRCh38 chr1: 93,168,389-93,169,779 , GRCh37.p13 chr1: 93,633,946-93,635,336 TMED5
    nsv6244378mobile element insertion1nstd215human GRCh38 chr1: 93,167,530-93,167,530 , GRCh37.p13 chr1: 93,633,087-93,633,087 TMED5
    nsv6133888copy number variation1nstd213human GRCh37 chr1: 93,020,000-94,900,001 , GRCh38.p12 chr1: 92,554,443-94,434,445 ABCA4, DR1, 47 more genes
    nsv6133783copy number variation1nstd213human GRCh37 chr1: 93,390,000-93,800,001 , GRCh38.p12 chr1: 92,924,443-93,334,444 MND1P1, RN7SL692P, 11 more genes
    nsv5882813copy number variation1nstd209human GRCh38 chr1: 93,168,562-93,169,773 , GRCh37.p13 chr1: 93,634,119-93,635,330 TMED5
    nsv5830849copy number variation1nstd209human GRCh38 chr1: 93,168,681-93,170,017 , GRCh37.p13 chr1: 93,634,238-93,635,574 TMED5
    nsv5690215mobile element insertion1nstd211human GRCh38 chr1: 93,178,882-93,178,882 , GRCh37.p13 chr1: 93,644,439-93,644,439 TMED5, CCDC18
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