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Items: 16

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    Number of Variants: 16

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097327copy number variation1nstd102humanPathogenic GRCh37 chr6: 30,890,861-30,892,357 , GRCh38.p12 chr6: 30,923,084-30,924,580 VARS2
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 VARS2, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 VARS2, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 VARS2, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 VARS2, ITPR3, 2905 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 VARS2, HLA-DPB2, 1001 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 VARS2, TRR-ACG1-2, 1385 more genes
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 VARS2, ABCF1, 313 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv3881292copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,860,807-30,957,425 , GRCh38.p12 chr6: 30,893,030-30,989,648 VARS2, GTF2H4, 6 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 VARS2, LEMD2, 321 more genes
    nsv3870570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590 VARS2, LOC105375002, 345 more genes
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 VARS2, HCG21, 117 more genes
    nsv3876127copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,384,577-31,902,308 , GRCh38.p12 chr6: 31,416,800-31,934,531 HCP5, SNORD48, 66 more genes
    nsv3921657copy number variation1nstd102humanUncertain significance NCBI36 chr6: 31,773,217-31,934,913 , GRCh37.p13 chr6|NT_167245.1: 2,950,808-3,112,520 , GRCh37.p13 chr6|NT_167247.1: 3,044,917-3,154,498 , GRCh37.p13 chr6|NT_167249.1: 3,054,967-3,159,682 , GRCh37.p13 chr6|NT_167244.1: 3,037,483-3,141,689 , GRCh37.p13 chr6: 31,665,238-31,826,934 , GRCh38.p12 chr6: 31,697,461-31,859,157 , GRCh38.p12 chr6|NT_167247.2: 3,039,332-3,148,913 , GRCh38.p12 chr6|NT_167249.2: 3,055,670-3,160,384 , GRCh38.p12 chr6|NT_167245.2: 2,945,223-3,106,935 , GRCh38.p12 chr6|NT_167244.2: 3,087,568-3,191,773 CLIC1, SAPCD1, 24 more genes
    nsv6314918copy number variation1nstd102humanUncertain significance GRCh38 chr6: 30,888,982-31,005,512 , GRCh37.p13 chr6: 30,856,759-30,973,289 VARS2, MUC21, 8 more genes
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