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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv6932054copy number variation1nstd229human GRCh38 chr13: 28,664,954-29,303,763 , GRCh37.p13 chr13: 29,239,091-29,877,900 CYP51A1P2, POM121L13P, 4 more genes
    nsv6929344copy number variation1nstd229human GRCh38 chr13: 28,557,101-29,389,500 , GRCh37.p13 chr13: 29,131,238-29,963,637 SLC46A3, MTUS2, 7 more genes
    nsv6928852copy number variation1nstd229human GRCh38 chr13: 28,406,460-28,885,623 , GRCh37.p13 chr13: 28,980,597-29,459,760 RNU6-53P, SLC46A3, 7 more genes
    nsv6922734copy number variation1nstd229human GRCh38 chr13: 28,712,301-28,725,200 , GRCh37.p13 chr13: 29,286,438-29,299,337 CYP51A1P2, SLC46A3
    nsv6920708copy number variation1nstd229human GRCh38 chr13: 28,708,942-28,713,359 , GRCh37.p13 chr13: 29,283,079-29,287,496 SLC46A3
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622039copy number variation1nstd224human GRCh37 chr13: 28,996,604-29,451,698 , GRCh38.p12 chr13: 28,422,467-28,877,561 FLT1, MTUS2, 7 more genes
    nsv6494437copy number variation1nstd223human GRCh38 chr13: 28,701,665-28,702,019 , GRCh37.p13 chr13: 29,275,802-29,276,156 SLC46A3, RNU6-53P
    nsv6490600copy number variation1nstd223human GRCh38 chr13: 28,714,131-28,714,523 , GRCh37.p13 chr13: 29,288,268-29,288,660 SLC46A3
    nsv6490259copy number variation1nstd223human GRCh38 chr13: 28,702,600-28,702,953 , GRCh37.p13 chr13: 29,276,737-29,277,090 RNU6-53P, SLC46A3
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6291749copy number variation1nstd102humanUncertain significance GRCh37 chr13: 29,125,286-29,976,823 , GRCh38.p12 chr13: 28,551,149-29,402,686 MTUS2, POM121L13P, 7 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6132637copy number variation1nstd213human GRCh37 chr13: 29,170,000-30,250,001 , GRCh38.p12 chr13: 28,595,863-29,675,864 GAPDHP69, SLC7A1, 9 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132475copy number variation1nstd213human GRCh37 chr13: 26,620,000-32,650,001 , GRCh38.p12 chr13: 26,045,862-32,075,864 ALOX5AP, HMGB1, 106 more genes
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
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