U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 19

    loading data ...

    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LTV1, LOC100131041, 146 more genes
    nsv3891146copy number variation1nstd102humanPathogenic GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095 LTV1, UST, 131 more genes
    nsv3916499copy number variation1nstd102humanPathogenic NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644 LTV1, SLC35D3, 127 more genes
    nsv3890752copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870 LTV1, LOC105378052, 109 more genes
    nsv3912178copy number variation1nstd102humanPathogenic NCBI36 chr6: 142,070,748-145,748,578 , GRCh37.p13 chr6: 142,029,055-145,706,885 , GRCh38.p12 chr6: 141,707,918-145,385,749 LTV1, GJE1, 40 more genes
    nsv7097046copy number variation1nstd102humanPathogenic GRCh37 chr6: 142,623,467-144,508,628 , GRCh38.p12 chr6: 142,302,330-144,187,491 LTV1, ZC2HC1B, 26 more genes
    nsv5673595copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,772,160-144,508,648 , GRCh38.p12 chr6: 143,451,023-144,187,511 LTV1, LOC105378036, 14 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LTV1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 LTV1, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 LTV1, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 LTV1, ITPR3, 2905 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LTV1, LOC105369171, 418 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 LTV1, KATNA1, 422 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 LTV1, UST-AS2, 394 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 LTV1, TPD52L1, 316 more genes
    nsv3911164copy number variation1nstd102humanPathogenic NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117 LTV1, HYMAI, 263 more genes
    nsv6313714copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,331,663-145,817,051 , GRCh38.p12 chr6: 143,010,526-145,495,915 LTV1, LOC100131041, 31 more genes
    nsv6313657copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,874,282-145,071,930 , GRCh38.p12 chr6: 143,553,145-144,750,794 LTV1, LOC105378036, 14 more genes
    nsv3921844copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,940,111-144,734,319 , GRCh38 chr6: 143,618,974-144,413,183 , NCBI36 chr6: 143,981,804-144,776,012 LTV1, ZC2HC1B, 13 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Search details

    See more...

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center