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Items: 1 to 20 of 273

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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
    nsv7067003inversion1nstd229human GRCh38 chr13: 52,739,716-52,792,713 , GRCh37.p13 chr13: 53,313,851-53,366,848 CNMD
    nsv6952879copy number variation1nstd229human GRCh38 chr13: 52,737,787-52,739,928 , GRCh37.p13 chr13: 53,311,922-53,314,063 CNMD
    nsv6948095copy number variation1nstd229human GRCh38 chr13: 52,739,701-52,789,500 , GRCh37.p13 chr13: 53,313,836-53,363,635 CNMD
    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
    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
    nsv6194202copy number variation1nstd214human GRCh38 chr13: 52,707,298-52,707,409 , GRCh37.p13 chr13: 53,281,433-53,281,544 CNMD
    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
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132500copy number variation1nstd213human GRCh37 chr13: 52,780,000-53,580,001 , GRCh38.p12 chr13: 52,205,865-53,005,866 PCDH8, SUGT1, 13 more genes
    nsv6092522insertion1nstd212human GRCh38 chr13: 52,712,924-52,712,924 , GRCh37.p13 chr13: 53,287,059-53,287,059 CNMD
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