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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076951inversion1nstd229human GRCh38 chr13: 53,922,877-55,143,098 , GRCh37.p13 chr13: 54,497,012-55,717,233 MIR1297, LOC105370213, 2 more genes
    nsv6952331copy number variation1nstd229human GRCh38 chr13: 53,971,288-54,276,329 , GRCh37.p13 chr13: 54,545,423-54,850,464 LINC00458
    nsv6949974copy number variation1nstd229human GRCh38 chr13: 53,971,367-54,273,374 , GRCh37.p13 chr13: 54,545,502-54,847,509 LINC00458
    nsv6946006copy number variation1nstd229human GRCh38 chr13: 54,119,610-54,127,406 , GRCh37.p13 chr13: 54,693,745-54,701,541 LINC00458
    nsv6945363copy number variation1nstd229human GRCh38 chr13: 54,069,087-56,405,225 , GRCh37.p13 chr13: 54,643,222-56,979,359 HNF4GP1, RPL13AP25, 6 more genes
    nsv6945076copy number variation1nstd229human GRCh38 chr13: 54,117,824-54,125,722 , GRCh37.p13 chr13: 54,691,959-54,699,857 LINC00458
    nsv6944297copy number variation1nstd229human GRCh38 chr13: 54,056,284-54,394,083 , GRCh37.p13 chr13: 54,630,419-54,968,218 MIR1297, LINC00458
    nsv6941503copy number variation1nstd229human GRCh38 chr13: 53,823,390-55,127,279 , GRCh37.p13 chr13: 54,397,525-55,701,414 LINC00558, LOC105370213, 3 more genes
    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
    nsv6475803copy number variation1nstd223human GRCh38 chr13: 54,009,227-55,519,960 , GRCh37.p13 chr13: 54,583,362-56,094,095 MIR5007, RPL13AP25, 3 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
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 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
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6290319copy number variation1nstd102humanPathogenic GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079 CNMD, CPB2-AS1, 241 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
    nsv6133100copy number variation1nstd213human GRCh37 chr13: 52,550,000-56,590,001 , GRCh38.p12 chr13: 51,975,864-56,015,867 ATP7B, NEK3, 34 more genes
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132560copy number variation1nstd213human GRCh37 chr13: 54,650,000-54,900,001 , GRCh38.p12 chr13: 54,075,865-54,325,866 MIR1297, LINC00458
    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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