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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145595insertion1nstd232human GRCh37.p13 chr13: 29,242,712-29,242,712 , GRCh38.p12 chr13: 28,668,575-28,668,575 POMP
    nsv7094472copy number variation1nstd102humanUncertain significance GRCh37 chr13: 29,252,152-29,252,239 , GRCh38.p12 chr13: 28,678,015-28,678,102 POMP
    nsv7093474insertion1nstd102humanUncertain significance GRCh38 chr13: 28,672,440-28,672,440 , GRCh37 chr13: 29,246,577-29,246,577 POMP
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv6936685copy number variation1nstd229human GRCh38 chr13: 28,654,501-28,661,900 , GRCh37.p13 chr13: 29,228,638-29,236,037 POMP
    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
    nsv6928090copy number variation1nstd229human GRCh38 chr13: 28,669,401-28,696,500 , GRCh37.p13 chr13: 29,243,538-29,270,637 POMP
    nsv6927246copy number variation1nstd229human GRCh38 chr13: 28,659,531-28,659,751 , GRCh37.p13 chr13: 29,233,668-29,233,888 POMP
    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
    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
    nsv6309503copy number variation1nstd102humanUncertain significance GRCh37 chr13: 29,233,226-29,233,344 , GRCh38.p12 chr13: 28,659,089-28,659,207 POMP
    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
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