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Items: 1 to 20 of 52

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312192copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,260,012-179,260,802 , GRCh38.p12 chr5: 179,833,012-179,833,802 , GRCh38.p12 chr5|NW_016107298.1: 598,572-599,362 SQSTM1
    nsv6311760copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,263,416-179,263,593 , GRCh38.p12 chr5: 179,836,416-179,836,593 , GRCh38.p12 chr5|NW_016107298.1: 601,976-602,153 SQSTM1, MRNIP
    nsv4683765copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,263,426-179,263,603 , GRCh38.p12 chr5: 179,836,426-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 601,986-602,163 SQSTM1, MRNIP
    nsv7097138copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,260,567-179,263,593 , GRCh38.p12 chr5|NW_016107298.1: 599,127-602,153 , GRCh38.p12 chr5: 179,833,567-179,836,593 SQSTM1, MRNIP
    nsv3888674copy number variation1nstd102humanBenign GRCh37 chr5: 179,219,357-179,240,499 , GRCh38.p12 chr5: 179,792,356-179,813,499 , GRCh38.p12 chr5|NW_016107298.1: 557,933-579,054 SQSTM1, MGAT4B, 2 more genes
    nsv1398443copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,397,487-180,686,444 , GRCh38.p12 chr5: 174,970,484-181,259,443 SQSTM1, TRV-AAC1-3, 203 more genes
    nsv3920109copy number variation1nstd102humanPathogenic NCBI36 chr5: 174,896,380-180,652,395 , GRCh37 chr5: 174,963,774-180,719,789 , GRCh38 chr5: 175,536,771-181,292,788 SQSTM1, LOC100289470, 198 more genes
    nsv3873295copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-180,719,789 , GRCh38.p12 chr5: 176,143,674-181,292,788 SQSTM1, LINC02222, 186 more genes
    nsv3922812copy number variation1nstd102humanPathogenic NCBI36 chr5: 176,059,735-180,629,412 , GRCh38 chr5: 176,700,128-181,269,805 , GRCh37 chr5: 176,127,129-180,696,806 SQSTM1, MRPL50P3, 167 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 SQSTM1, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 SQSTM1, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SQSTM1, SPEF2, 2490 more genes
    nsv3874238copy number variation1nstd102humanPathogenic GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337 SQSTM1, PJA2, 1228 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 SQSTM1, GRM6, 554 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 SQSTM1, RN7SKP148, 553 more genes
    nsv3885523copy number variation1nstd102humanPathogenic GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343 SQSTM1, WWC1, 446 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 SQSTM1, CEP192P1, 443 more genes
    nsv3921186copy number variation1nstd102humanPathogenic GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412 SQSTM1, TENM2, 347 more genes
    nsv3920339copy number variation1nstd102humanPathogenic NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805 SQSTM1, MIR1229, 343 more genes
    nsv3918887copy number variation1nstd102humanPathogenic GRCh37 chr5: 168,761,759-180,712,302 , NCBI36 chr5: 168,694,337-180,644,908 , GRCh38 chr5: 169,334,755-181,285,301 SQSTM1, RPS8P7, 311 more genes
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