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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096762copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr5: 155,338,082-156,899,968 , GRCh38.p12 chr5: 155,911,072-157,472,960 NIPAL4, RNU6-556P, 14 more genes
    nsv7057012inversion1nstd229human GRCh38 chr5: 156,491,921-156,874,286 , GRCh37.p13 chr5: 155,918,931-156,301,297 LOC105377673, SGCD, 2 more genes
    nsv7052590inversion1nstd229human GRCh38 chr5: 154,695,187-159,271,728 , GRCh37.p13 chr5: 154,074,747-158,698,736 MRPL22, LOC105377673, 58 more genes
    nsv6783496copy number variation1nstd229human GRCh38 chr5: 156,444,258-156,869,855 , GRCh37.p13 chr5: 155,871,268-156,296,866 SGCD, PPP1R2B, 2 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6557338inversion1nstd223human GRCh38 chr5: 156,491,921-156,874,287 , GRCh37.p13 chr5: 155,918,931-156,301,298 SGCD, PPP1R2B, 2 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6312284copy number variation1nstd102humanUncertain significance GRCh37 chr5: 155,935,591-156,899,968 , GRCh38.p12 chr5: 156,508,581-157,472,960 TIMD4, HAVCR1, 14 more genes
    nsv6295598copy number variation1nstd186human GRCh37 chr5: 156,266,556-156,482,069 , GRCh38.p12 chr5: 156,839,545-157,055,058 HAVCR1, TIMD4, 2 more genes
    nsv6290966copy number variation1nstd102humannot provided GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573 C1QTNF2, MED7, 86 more genes
    nsv6135388copy number variation1nstd213human GRCh37 chr5: 153,010,000-160,030,001 , GRCh38.p12 chr5: 153,630,440-160,602,994 ADRA1B, EBF1, 107 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5456725copy number variation1nstd206human GRCh38 chr5: 156,839,545-157,055,058 , GRCh37.p13 chr5: 156,266,556-156,482,069 HAVCR1, PPP1R2B, 2 more genes
    nsv5087896mobile element insertion1nstd203human GRCh38 chr5: 156,849,515-156,849,527 , GRCh37.p13 chr5: 156,276,526-156,276,538 PPP1R2B
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
    nsv3922783copy number variation1nstd102humanPathogenic GRCh38 chr5: 152,761,187-167,248,053 , NCBI36 chr5: 152,120,940-166,607,636 , GRCh37 chr5: 152,140,747-166,675,058 APOOP1, LOC102724458, 151 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3915958copy number variation1nstd102humanPathogenic GRCh38 chr5: 152,443,869-166,104,392 , NCBI36 chr5: 151,803,623-165,463,975 , GRCh37 chr5: 151,823,430-165,531,397 C5orf52, FAM114A2, 147 more genes
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