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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6797329copy number variation1nstd229human GRCh38 chr5: 170,308,797-170,456,558 , GRCh37.p13 chr5: 169,735,801-169,883,562 KCNIP1, KCNIP1-OT1, 3 more genes
    nsv6796240copy number variation1nstd229human GRCh38 chr5: 170,378,976-170,383,678 , GRCh37.p13 chr5: 169,805,980-169,810,682 KCNIP1, KCNMB1
    nsv6794600copy number variation1nstd229human GRCh38 chr5: 170,379,720-170,387,215 , GRCh37.p13 chr5: 169,806,724-169,814,219 KCNIP1, KCNMB1
    nsv6794585copy number variation1nstd229human GRCh38 chr5: 170,367,765-170,571,170 , GRCh37.p13 chr5: 169,794,769-169,998,174 KCNIP1, KCNIP1-OT1, 1 more genes
    nsv6791807copy number variation1nstd229human GRCh38 chr5: 170,383,303-170,383,467 , GRCh37.p13 chr5: 169,810,307-169,810,471 KCNIP1, KCNMB1
    nsv6784394copy number variation1nstd229human GRCh38 chr5: 170,367,087-170,376,874 , GRCh37.p13 chr5: 169,794,091-169,803,878 KCNIP1, KCNMB1
    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
    nsv6636414copy number variation1nstd102humanUncertain significance GRCh37 chr5: 169,679,354-170,242,652 , GRCh38.p12 chr5: 170,252,350-170,815,648 GABRP, KCNIP1-OT1, 10 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
    nsv6181890copy number variation1nstd214human GRCh38 chr5: 170,375,560-170,375,613 , GRCh37.p13 chr5: 169,802,564-169,802,617 KCNIP1, KCNMB1
    nsv6174684copy number variation1nstd214human GRCh38 chr5: 170,375,533-170,375,586 , GRCh37.p13 chr5: 169,802,537-169,802,590 KCNMB1, KCNIP1
    nsv6136095copy number variation1nstd213human GRCh37 chr5: 169,340,000-169,870,001 , GRCh38.p12 chr5: 169,912,996-170,442,997 DOCK2, FOXI1, 11 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 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
    nsv6002773copy number variation1nstd212human GRCh38 chr5: 170,375,560-170,375,614 , GRCh37.p13 chr5: 169,802,564-169,802,618 KCNIP1, KCNMB1
    nsv5902584copy number variation1nstd209human GRCh38 chr5: 170,274,293-170,534,408 , GRCh37.p13 chr5: 169,701,297-169,961,412 KCNMB1, LCP2, 4 more genes
    nsv5901915copy number variation1nstd209human GRCh38 chr5: 170,375,560-170,375,613 , GRCh37.p13 chr5: 169,802,564-169,802,617 KCNIP1, KCNMB1
    nsv5842118copy number variation1nstd209human GRCh38 chr5: 170,362,578-170,434,914 , GRCh37.p13 chr5: 169,789,582-169,861,918 KCNIP1, KCNMB1, 1 more genes
    nsv5841571copy number variation1nstd209human GRCh38 chr5: 170,373,383-170,374,382 , GRCh37.p13 chr5: 169,800,387-169,801,386 KCNMB1, KCNIP1
    nsv5578580copy number variation1nstd207human GRCh38 chr5: 170,375,560-170,375,613 , GRCh37.p13 chr5: 169,802,564-169,802,617 KCNMB1, KCNIP1
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