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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6973635copy number variation1nstd229human GRCh38 chr15: 70,581,051-70,581,129 , GRCh37.p13 chr15: 70,873,390-70,873,468 LINC02204
    nsv6972406copy number variation1nstd229human GRCh38 chr15: 70,585,244-70,588,797 , GRCh37.p13 chr15: 70,877,583-70,881,136 LINC02204
    nsv6970675copy number variation1nstd229human GRCh38 chr15: 70,504,471-70,657,149 , GRCh37.p13 chr15: 70,796,810-70,949,488 LINC02204, UACA, 5 more genes
    nsv6968199copy number variation1nstd229human GRCh38 chr15: 70,586,336-70,586,437 , GRCh37.p13 chr15: 70,878,675-70,878,776 LINC02204
    nsv6961707copy number variation1nstd229human GRCh38 chr15: 70,585,628-70,617,903 , GRCh37.p13 chr15: 70,877,967-70,910,242 LINC02204, SALRNA3
    nsv6961113copy number variation1nstd229human GRCh38 chr15: 70,570,823-70,609,640 , GRCh37.p13 chr15: 70,863,162-70,901,979 LINC02204
    nsv6637906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 68,807,665-70,981,473 , GRCh38.p12 chr15: 68,515,326-70,689,134 UACA, RPLP1, 36 more genes
    nsv6637504copy number variation1nstd102humanUncertain significance GRCh37 chr15: 70,814,037-71,028,303 , GRCh38.p12 chr15: 70,521,698-70,735,964 SALRNA2, LINC02204, 4 more genes
    nsv6584403inversion1nstd223human GRCh38 chr15: 70,570,097-70,570,649 , GRCh37.p13 chr15: 70,862,436-70,862,988 LINC02204
    nsv6498258copy number variation1nstd223human GRCh38 chr15: 70,585,244-70,588,791 , GRCh37.p13 chr15: 70,877,583-70,881,130 LINC02204
    nsv6132961copy number variation1nstd213human GRCh37 chr15: 69,080,000-73,430,001 , GRCh38.p12 chr15: 68,787,661-73,137,660 BBS4, MYO9A, 84 more genes
    nsv5933825copy number variation1nstd209human GRCh38 chr15: 70,581,051-70,581,128 , GRCh37.p13 chr15: 70,873,390-70,873,467 LINC02204
    nsv5530731copy number variation1nstd206human GRCh38 chr15: 70,581,051-70,581,129 , GRCh37.p13 chr15: 70,873,390-70,873,468 LINC02204
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5311441copy number variation1nstd204human GRCh38.p13 chr15: 70,577,302-70,579,130 , GRCh37.p13 chr15: 70,869,641-70,871,469 LINC02204
    nsv5142712mobile element insertion1nstd203human GRCh38 chr15: 70,569,986-70,569,998 , GRCh37.p13 chr15: 70,862,325-70,862,337 LINC02204
    nsv5005549copy number variation1nstd200human GRCh38 chr15: 70,577,511-70,579,014 , GRCh37.p13 chr15: 70,869,850-70,871,353 LINC02204
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