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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097266copy number variation1nstd102humanPathogenic GRCh37 chr5: 167,849,013-169,661,202 , GRCh38.p12 chr5: 168,422,008-170,234,198 FBLL1, RNU6-477P, 25 more genes
    nsv7056659inversion1nstd229human GRCh38 chr5: 169,919,774-169,924,772 , GRCh37.p13 chr5: 169,346,778-169,351,776 INSYN2B, DOCK2
    nsv7052523inversion1nstd229human GRCh38 chr5: 169,919,771-169,919,813 , GRCh37.p13 chr5: 169,346,775-169,346,817 INSYN2B, DOCK2
    nsv7052493inversion1nstd229human GRCh38 chr5: 169,867,601-169,867,635 , GRCh37.p13 chr5: 169,294,605-169,294,639 DOCK2, INSYN2B
    nsv7046323inversion1nstd229human GRCh38 chr5: 169,130,180-169,938,954 , GRCh37.p13 chr5: 168,557,185-169,365,958 SLIT3, DOCK2, 6 more genes
    nsv7039162inversion1nstd229human GRCh38 chr5: 169,863,243-169,863,270 , GRCh37.p13 chr5: 169,290,247-169,290,274 INSYN2B, DOCK2
    nsv6796771copy number variation1nstd229human GRCh38 chr5: 169,938,743-169,944,250 , GRCh37.p13 chr5: 169,365,747-169,371,254 INSYN2B, DOCK2
    nsv6794946copy number variation1nstd229human GRCh38 chr5: 169,910,540-169,910,567 , GRCh37.p13 chr5: 169,337,544-169,337,571 DOCK2, INSYN2B
    nsv6792980copy number variation1nstd229human GRCh38 chr5: 169,953,890-169,961,193 , GRCh37.p13 chr5: 169,380,894-169,388,197 INSYN2B, DOCK2
    nsv6791654copy number variation1nstd229human GRCh38 chr5: 169,865,084-169,869,585 , GRCh37.p13 chr5: 169,292,088-169,296,589 INSYN2B, DOCK2
    nsv6790392copy number variation1nstd229human GRCh38 chr5: 169,939,094-169,941,396 , GRCh37.p13 chr5: 169,366,098-169,368,400 INSYN2B, DOCK2
    nsv6790239copy number variation1nstd229human GRCh38 chr5: 169,925,701-169,948,500 , GRCh37.p13 chr5: 169,352,705-169,375,504 INSYN2B, DOCK2
    nsv6787829copy number variation1nstd229human GRCh38 chr5: 169,935,787-169,941,332 , GRCh37.p13 chr5: 169,362,791-169,368,336 INSYN2B, DOCK2
    nsv6786439copy number variation1nstd229human GRCh38 chr5: 169,955,695-169,959,622 , GRCh37.p13 chr5: 169,382,699-169,386,626 INSYN2B, DOCK2
    nsv6786367copy number variation1nstd229human GRCh38 chr5: 169,678,352-169,946,919 , GRCh37.p13 chr5: 169,105,356-169,373,923 INSYN2B, DOCK2
    nsv6785905copy number variation1nstd229human GRCh38 chr5: 169,960,101-169,962,900 , GRCh37.p13 chr5: 169,387,105-169,389,904 DOCK2, INSYN2B
    nsv6783611copy number variation1nstd229human GRCh38 chr5: 169,911,163-169,942,974 , GRCh37.p13 chr5: 169,338,167-169,369,978 INSYN2B, DOCK2
    nsv6783495copy number variation1nstd229human GRCh38 chr5: 169,869,563-169,869,599 , GRCh37.p13 chr5: 169,296,567-169,296,603 DOCK2, INSYN2B
    nsv6782140copy number variation1nstd229human GRCh38 chr5: 169,972,535-169,975,997 , GRCh37.p13 chr5: 169,399,539-169,403,001 INSYN2B, DOCK2
    nsv6781147copy number variation1nstd229human GRCh38 chr5: 169,873,808-169,874,164 , GRCh37.p13 chr5: 169,300,812-169,301,168 DOCK2, INSYN2B
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