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Items: 1 to 20 of 585

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146368copy number variation1nstd232human GRCh37.p13 chr2: 24,474,352-24,474,409 , GRCh38.p12 chr2: 24,251,483-24,251,540 ITSN2
    nsv7143783insertion1nstd232human GRCh37.p13 chr2: 24,487,570-24,487,570 , GRCh38.p12 chr2: 24,264,701-24,264,701 ITSN2
    nsv7138697insertion1nstd232human GRCh37.p13 chr2: 24,487,544-24,487,544 , GRCh38.p12 chr2: 24,264,675-24,264,675 ITSN2
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096411copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,443,763-26,029,226 , GRCh38.p12 chr2: 24,220,894-25,806,357 LOC105369164, DTNB-AS1, 24 more genes
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv7042930inversion1nstd229human GRCh38 chr2: 24,288,779-24,291,927 , GRCh37.p13 chr2: 24,511,648-24,514,796 ITSN2
    nsv7038666inversion1nstd229human GRCh38 chr2: 24,352,691-24,355,039 , GRCh37.p13 chr2: 24,575,560-24,577,908 ITSN2
    nsv6676842copy number variation1nstd229human GRCh38 chr2: 24,338,885-24,339,110 , GRCh37.p13 chr2: 24,561,754-24,561,979 ITSN2
    nsv6676012copy number variation1nstd229human GRCh38 chr2: 24,216,705-24,217,118 , GRCh37.p13 chr2: 24,439,574-24,439,987 ITSN2
    nsv6675310copy number variation1nstd229human GRCh38 chr2: 24,325,312-24,330,653 , GRCh37.p13 chr2: 24,548,181-24,553,522 ITSN2, HMGN2P20
    nsv6674792copy number variation1nstd229human GRCh38 chr2: 24,210,638-24,214,615 , GRCh37.p13 chr2: 24,433,507-24,437,484 ITSN2
    nsv6674629copy number variation1nstd229human GRCh38 chr2: 24,323,879-25,622,192 , GRCh37.p13 chr2: 24,546,748-25,845,061 POMC, RNA5SP88, 22 more genes
    nsv6674189copy number variation1nstd229human GRCh38 chr2: 24,202,627-24,202,780 , GRCh37.p13 chr2: 24,425,496-24,425,649 ITSN2
    nsv6673810copy number variation1nstd229human GRCh38 chr2: 24,194,701-24,203,000 , GRCh37.p13 chr2: 24,417,570-24,425,869 ITSN2
    nsv6673456copy number variation1nstd229human GRCh38 chr2: 24,320,901-24,338,600 , GRCh37.p13 chr2: 24,543,770-24,561,469 ITSN2, HMGN2P20, 1 more genes
    nsv6669007copy number variation1nstd229human GRCh38 chr2: 24,360,701-24,494,700 , GRCh37.p13 chr2: 24,583,570-24,717,569 NCOA1, LOC105374329, 1 more genes
    nsv6667818copy number variation1nstd229human GRCh38 chr2: 24,334,733-24,345,307 , GRCh37.p13 chr2: 24,557,602-24,568,176 RPL36AP13, ITSN2
    nsv6667195copy number variation1nstd229human GRCh38 chr2: 24,353,734-24,356,173 , GRCh37.p13 chr2: 24,576,603-24,579,042 ITSN2
    nsv6666191copy number variation1nstd229human GRCh38 chr2: 24,329,838-24,343,170 , GRCh37.p13 chr2: 24,552,707-24,566,039 HMGN2P20, RPL36AP13, 1 more genes
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