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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067898inversion1nstd229human GRCh38 chr13: 52,258,187-52,716,407 , GRCh37.p13 chr13: 52,832,322-53,290,542 HNRNPA1L2, CKAP2, 10 more genes
    nsv7065247inversion1nstd229human GRCh38 chr13: 52,221,056-52,665,291 , GRCh37.p13 chr13: 52,795,191-53,239,426 TPTE2P3, LOC105370207, 9 more genes
    nsv6948726copy number variation1nstd229human GRCh38 chr13: 52,611,549-52,652,260 , GRCh37.p13 chr13: 53,185,684-53,226,395 SUGT1, HNRNPA1L2
    nsv6943389copy number variation1nstd229human GRCh38 chr13: 52,668,371-52,671,648 , GRCh37.p13 chr13: 53,242,506-53,245,783 SUGT1
    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
    nsv6577057inversion1nstd223human GRCh38 chr13: 52,680,987-52,681,406 , GRCh37.p13 chr13: 53,255,122-53,255,541 SUGT1
    nsv6485848copy number variation1nstd223human GRCh38 chr13: 52,671,201-52,673,000 , GRCh37.p13 chr13: 53,245,336-53,247,135 SUGT1
    nsv6484909copy number variation1nstd223human GRCh38 chr13: 52,611,301-52,652,300 , GRCh37.p13 chr13: 53,185,436-53,226,435 SUGT1, HNRNPA1L2
    nsv6479339copy number variation1nstd223human GRCh38 chr13: 52,676,474-52,677,328 , GRCh37.p13 chr13: 53,250,609-53,251,463 SUGT1
    nsv6315497copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,535,544-53,362,733 , GRCh38.p12 chr13: 51,961,408-52,788,598 HNRNPA1L2, NEK3, 19 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
    nsv6314198copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002 PCNPP5, NRAD1, 189 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
    nsv6314000copy number variation1nstd102humanUncertain significance GRCh37 chr13: 53,245,555-53,328,934 , GRCh38.p12 chr13: 52,671,420-52,754,799 SUGT1, CNMD
    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
    nsv6249076mobile element insertion1nstd215human GRCh38 chr13: 52,675,776-52,675,776 , GRCh37.p13 chr13: 53,249,911-53,249,911 SUGT1
    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
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