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Items: 1 to 20 of 23

  • The following term was not found in dbVar: histone.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3875385copy number variation1nstd102humanBenign GRCh37 chr6: 27,093,821-27,158,033 , GRCh38.p12 chr6: 27,126,042-27,190,254 H2AC12, TRH-GTG1-5, 8 more genes
    nsv3911053copy number variation1nstd102humanUncertain significance GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069 GPX5, TRI-AAT9-1, 232 more genes
    nsv1398184copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,545,571-27,115,102 , GRCh38.p12 chr6: 26,545,343-27,147,323 TRM-CAT4-2, VN1R12P, 41 more genes
    nsv3873727copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,928,203-27,344,831 , GRCh38.p12 chr6: 26,960,424-27,377,052 TRV-CAC6-1, CDCA7P1, 42 more genes
    nsv429572copy number variation1nstd11human GRCh38.p12 chr6: 149,661-170,741,917 , NCBI36 chr6: 94,661-170,892,930 , GRCh37.p13 chr6: 149,661-171,051,005 ABCF1, ACAT2, 3006 more genes
    nsv429610copy number variation1nstd11human NCBI36 chr6: 110,632-42,839,093 , GRCh37.p13 chr6: 165,632-42,731,115 , GRCh38.p12 chr6: 165,632-42,763,377 ABCF1, AGER, 1322 more genes
    nsv482235copy number variation1nstd40human GRCh37 chr6: 25,200,001-30,400,000 , GRCh38.p12 chr6: 25,199,773-30,432,223 BTN1A1, GABBR1, 449 more genes
    nsv6135506copy number variation1nstd213human GRCh37 chr6: 27,060,000-27,130,001 , GRCh38.p12 chr6: 27,092,221-27,162,222 H4C9, H2AC11, 10 more genes
    nsv948921copy number variation1nstd85human NCBI35 chr6: 26,664,869-27,551,936 , GRCh37.p13 chr6: 26,556,890-27,443,957 , GRCh38.p12 chr6: 26,556,662-27,476,178 TRI-AAT9-1, ZNF184, 71 more genes
    nsv4381128copy number variation1nstd173human GRCh37 chr6: 26,941,502-27,391,254 , GRCh38.p12 chr6: 26,973,723-27,423,475 RPL10P2, H2BC11, 45 more genes
    esv4010739copy number variation1estd233human GRCh37 chr6: 24,161,000-29,728,000 , GRCh38.p12 chr6: 24,160,772-29,760,223 BTN1A1, GABBR1, 420 more genes
    nsv538047copy number variation1nstd54human NCBI36 chr6: 128,203-32,252,909 , GRCh37.p13 chr6: 183,203-32,144,931 , GRCh38.p12 chr6: 183,203-32,177,154 VN1R14P, HLA-H, 1014 more genes
    nsv538068copy number variation1nstd54human NCBI36 chr6: 334,422-31,064,339 , GRCh37.p13 chr6: 389,422-30,956,360 , GRCh38.p12 chr6: 389,422-30,988,583 GCM2, LOC105374953, 888 more genes
    nsv2768223copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr6: 26,096,965-29,385,631 , GRCh37 chr6: 26,097,193-29,353,408 BTN1A1, GPX5, 329 more genes
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