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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6834298copy number variation1nstd229human GRCh38 chr7: 55,769,234-56,068,384 , GRCh37.p13 chr7: 55,836,927-56,136,077 ZNF713, LOC101409255, 12 more genes
    nsv6824671copy number variation1nstd229human GRCh38 chr7: 55,955,935-55,963,258 , GRCh37.p13 chr7: 56,023,628-56,030,951 MRPS17, NIPSNAP2
    nsv6823936copy number variation1nstd229human GRCh38 chr7: 55,948,883-55,950,535 , GRCh37.p13 chr7: 56,016,576-56,018,228 MRPS17
    nsv6823794copy number variation1nstd229human GRCh38 chr7: 55,713,901-56,129,100 , GRCh37.p13 chr7: 55,781,594-56,196,793 SEPTIN14, LOC100419984, 23 more genes
    nsv6821297copy number variation1nstd229human GRCh38 chr7: 55,943,844-55,964,066 , GRCh37.p13 chr7: 56,011,537-56,031,759 MRPS17, NIPSNAP2
    nsv6636595copy number variation1nstd102humanUncertain significance GRCh37 chr7: 53,991,820-56,148,011 , GRCh38.p12 chr7: 53,924,127-56,080,318 PSPH, SNORA22B, 46 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6601321copy number variation1nstd223human GRCh38 chr7: 55,945,603-55,953,637 , GRCh37.p13 chr7: 56,013,296-56,021,330 MRPS17
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6291282copy number variation1nstd102humannot provided GRCh37 chr7: 55,952,277-56,022,846 , GRCh38.p12 chr7: 55,884,584-55,955,153 ZNF713, MRPS17
    nsv6291152copy number variation1nstd102humanLikely benign GRCh37 chr7: 55,757,106-56,489,653 , GRCh38.p12 chr7: 55,689,413-56,421,960 MRPS17, CCT6A, 43 more genes
    nsv6291142copy number variation1nstd102humanLikely benign GRCh37 chr7: 55,776,531-56,393,852 , GRCh38.p12 chr7: 55,708,838-56,326,159 SNORA15, CICP12, 29 more genes
    nsv6136192copy number variation1nstd213human GRCh37 chr7: 54,300,000-56,060,001 , GRCh38.p12 chr7: 54,232,307-55,992,308 EGFR, SLC25A5P3, 39 more genes
    nsv6111740inversion1nstd212human GRCh38 chr7: 55,763,050-56,016,250 , GRCh37.p13 chr7: 55,830,743-56,083,943 NIPSNAP2, PSPH, 8 more genes
    nsv6013062copy number variation1nstd212human GRCh38 chr7: 55,741,191-56,375,181 , GRCh37.p13 chr7: 55,808,884-56,442,874 , PSPH, 36 more genes
    nsv5924366copy number variation1nstd209human GRCh38 chr7: 55,952,451-55,952,749 , GRCh37.p13 chr7: 56,020,144-56,020,442 MRPS17
    nsv5913713copy number variation1nstd209human GRCh38 chr7: 55,950,166-55,950,730 , GRCh37.p13 chr7: 56,017,859-56,018,423 MRPS17
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5477528copy number variation1nstd206human GRCh38 chr7: 55,282,120-56,410,000 , GRCh37.p13 chr7: 55,349,813-56,477,693 , MRPS17, 52 more genes
    nsv5237654copy number variation1nstd204human GRCh38.p13 chr7: 55,753,801-56,067,900 , GRCh37.p13 chr7: 55,821,494-56,135,593 ZNF713, SUMF2, 13 more genes
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