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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070608inversion1nstd229human GRCh38 chr13: 37,808,702-41,386,678 , GRCh37.p13 chr13: 38,382,839-41,960,814 FREM2-AS1, SUGT1P3, 63 more genes
    nsv7065141inversion1nstd229human GRCh38 chr13: 38,333,904-38,621,420 , GRCh37.p13 chr13: 38,908,041-39,195,557 UFM1, LOC105370167, 3 more genes
    nsv6956544copy number variation1nstd229human GRCh38 chr13: 37,944,230-38,730,079 , GRCh37.p13 chr13: 38,518,367-39,304,216 PRDX3P3, LINC00437, 7 more genes
    nsv6953969copy number variation1nstd229human GRCh38 chr13: 38,356,976-38,357,050 , GRCh37.p13 chr13: 38,931,113-38,931,187 UFM1
    nsv6941951copy number variation1nstd229human GRCh38 chr13: 38,198,441-39,401,517 , GRCh37.p13 chr13: 38,772,578-39,975,654 NXT1P1, LOC105370168, 17 more genes
    nsv6941019copy number variation1nstd229human GRCh38 chr13: 38,349,201-38,350,400 , GRCh37.p13 chr13: 38,923,338-38,924,537 UFM1
    nsv6938199copy number variation1nstd229human GRCh38 chr13: 38,003,120-38,748,580 , GRCh37.p13 chr13: 38,577,257-39,322,717 FREM2, PRDX3P3, 6 more genes
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 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
    nsv6491552copy number variation1nstd223human GRCh38 chr13: 38,352,501-38,353,700 , GRCh37.p13 chr13: 38,926,638-38,927,837 UFM1
    nsv6488316copy number variation1nstd223human GRCh38 chr13: 38,348,069-38,348,349 , GRCh37.p13 chr13: 38,922,206-38,922,486 UFM1
    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
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6133091copy number variation1nstd213human GRCh37 chr13: 38,700,000-39,040,001 , GRCh38.p12 chr13: 38,125,863-38,465,864 UFM1, LINC00571
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132554copy number variation1nstd213human GRCh37 chr13: 38,850,000-39,030,001 , GRCh38.p12 chr13: 38,275,863-38,455,864 UFM1
    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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