U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv6987532copy number variation1nstd229human GRCh38 chr17: 63,844,221-63,856,627 , GRCh37.p13 chr17: 61,921,581-61,933,987 TCAM1P
    nsv6979306copy number variation1nstd229human GRCh38 chr17: 63,863,152-63,886,672 , GRCh37.p13 chr17: 61,940,512-61,964,032 CSH2, GH2, 1 more genes
    nsv6637179copy number variation1nstd102humanUncertain significance GRCh37 chr17: 61,838,634-62,465,444 , GRCh38.p12 chr17: 63,761,274-64,469,327 GH2, DDX42, 24 more genes
    nsv6624098copy number variation1nstd224human GRCh37 chr17: 61,912,893-61,977,248 , GRCh38.p12 chr17: 63,835,533-63,899,888 CSH2, SMARCD2, 3 more genes
    nsv6526795copy number variation1nstd223human GRCh38 chr17: 63,863,444-63,901,765 , GRCh37.p13 chr17: 61,940,804-61,979,125 TCAM1P, CSH1, 2 more genes
    nsv6517090copy number variation1nstd223human GRCh38 chr17: 63,863,768-63,887,339 , GRCh37.p13 chr17: 61,941,128-61,964,699 CSH2, TCAM1P, 1 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6023007copy number variation1nstd212human GRCh38 chr17: 63,864,416-63,864,742 , GRCh37.p13 chr17: 61,941,776-61,942,102 TCAM1P
    nsv5941062copy number variation1nstd209human GRCh38 chr17: 63,864,271-63,902,632 , GRCh37.p13 chr17: 61,941,631-61,979,992 , CSH1, 3 more genes
    nsv5877190copy number variation1nstd209human GRCh38 chr17: 63,864,243-63,877,288 , GRCh37.p13 chr17: 61,941,603-61,954,648 TCAM1P, CSH2
    nsv5602131copy number variation1nstd207human GRCh38 chr17: 63,864,420-63,864,731 , GRCh37.p13 chr17: 61,941,780-61,942,091 TCAM1P
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5295473copy number variation1nstd204human GRCh38.p13 chr17: 63,863,201-63,885,900 , GRCh37.p13 chr17: 61,940,561-61,963,260 , TCAM1P, 2 more genes
    nsv5293628copy number variation1nstd204human GRCh38.p13 chr17: 63,857,413-63,885,556 , GRCh37.p13 chr17: 61,934,773-61,962,916 , GH2, 2 more genes
    nsv5292062copy number variation1nstd204human GRCh38.p13 chr17: 63,540,501-63,873,300 , GRCh37.p13 chr17: 61,617,862-61,950,660 , KCNH6, 18 more genes
    nsv4851636copy number variation1nstd200human GRCh37 chr17: 61,941,700-61,980,030 , GRCh38.p12 chr17: 63,864,340-63,902,670 , GH2, 3 more genes
    nsv4851635copy number variation1nstd200human GRCh37 chr17: 61,941,724-61,965,219 , GRCh38.p12 chr17: 63,864,364-63,887,859 , CSH2, 2 more genes
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4418607copy number variation1nstd174human GRCh37 chr17: 61,941,021-61,971,802 , GRCh38.p12 chr17: 63,863,661-63,894,442 , CSH2, 3 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center