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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094410copy number variation1nstd102humanUncertain significance GRCh37 chr13: 51,484,213-52,602,726 , GRCh38.p12 chr13: 50,910,077-52,028,590 ATP7B, RNA5SP29, 29 more genes
    nsv7094084copy number variation1nstd102humanPathogenic GRCh37 chr13: 52,508,892-52,585,473 , GRCh38.p12 chr13: 51,934,756-52,011,337 FABP5P2, ALG11, 1 more genes
    nsv6955933copy number variation1nstd229human GRCh38 chr13: 51,936,045-52,031,550 , GRCh37.p13 chr13: 52,510,181-52,605,686 UTP14C, ALG11, 2 more genes
    nsv6953997copy number variation1nstd229human GRCh38 chr13: 52,004,352-52,126,041 , GRCh37.p13 chr13: 52,578,488-52,700,177 ATP7B, NEK5, 2 more genes
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6951676copy number variation1nstd229human GRCh38 chr13: 51,999,001-52,025,200 , GRCh37.p13 chr13: 52,573,137-52,599,336 UTP14C, ATP7B, 1 more genes
    nsv6949847copy number variation1nstd229human GRCh38 chr13: 52,024,714-52,030,768 , GRCh37.p13 chr13: 52,598,850-52,604,904 ALG11, UTP14C
    nsv6941985copy number variation1nstd229human GRCh38 chr13: 51,745,017-52,075,317 , GRCh37.p13 chr13: 52,319,153-52,649,453 UTP14C, DHRS12, 9 more genes
    nsv6938473copy number variation1nstd229human GRCh38 chr13: 51,742,952-52,015,459 , GRCh37.p13 chr13: 52,317,088-52,589,595 DHRS12, WDFY2, 7 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
    nsv6493355copy number variation1nstd223human GRCh38 chr13: 52,004,352-52,126,037 , GRCh37.p13 chr13: 52,578,488-52,700,173 ALG11, ATP7B, 2 more genes
    nsv6489538copy number variation1nstd223human GRCh38 chr13: 51,745,101-52,075,300 , GRCh37.p13 chr13: 52,319,237-52,649,436 UTP14C, NEK5, 9 more genes
    nsv6483285copy number variation1nstd223human GRCh38 chr13: 52,028,234-52,090,140 , GRCh37.p13 chr13: 52,602,370-52,664,276 UTP14C, NEK5, 1 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
    nsv6314657copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 52,549,305-52,585,631 , GRCh38.p12 chr13: 51,975,169-52,011,495 ATP7B, ALG11
    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
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