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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099256copy number variation1nstd231human GRCh38.p12 chr1: 201,916,209-203,311,623 , GRCh37 chr1: 201,885,337-203,280,751 ADORA1, CHI3L1, 49 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6300197copy number variation1nstd186human GRCh37 chr1: 203,275,201-203,275,327 , GRCh38.p12 chr1: 203,306,073-203,306,199 BTG2
    nsv6133960copy number variation1nstd213human GRCh37 chr1: 196,820,000-204,810,001 , GRCh38.p12 chr1: 196,850,870-204,840,873 ELF3, NR5A2, 181 more genes
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133846copy number variation1nstd213human GRCh37 chr1: 203,140,000-205,920,001 , GRCh38.p12 chr1: 203,170,872-205,950,873 CHIT1, ELK4, 90 more genes
    nsv6133845copy number variation1nstd213human GRCh37 chr1: 203,110,000-203,280,001 , GRCh38.p12 chr1: 203,140,872-203,310,873 ADORA1, CHI3L1, 6 more genes
    nsv6133584copy number variation1nstd213human GRCh37 chr1: 202,800,000-203,520,001 , GRCh38.p12 chr1: 202,830,872-203,550,873 ADORA1, OPTC, 29 more genes
    nsv5887076copy number variation1nstd209human GRCh38 chr1: 203,307,780-203,307,940 , GRCh37.p13 chr1: 203,276,908-203,277,068 BTG2
    nsv5872166copy number variation1nstd209human GRCh38 chr1: 203,306,446-203,306,596 , GRCh37.p13 chr1: 203,275,574-203,275,724 BTG2
    nsv5568768copy number variation1nstd207human GRCh38 chr1: 203,306,072-203,306,196 , GRCh37.p13 chr1: 203,275,200-203,275,324 BTG2
    nsv5447238copy number variation1nstd206human GRCh38 chr1: 203,306,297-203,306,429 , GRCh37.p13 chr1: 203,275,425-203,275,557 BTG2
    nsv5446597copy number variation1nstd206human GRCh38 chr1: 203,305,945-203,305,996 , GRCh37.p13 chr1: 203,275,073-203,275,124 BTG2
    nsv5444994copy number variation1nstd206human GRCh38 chr1: 203,306,073-203,306,199 , GRCh37.p13 chr1: 203,275,201-203,275,327 BTG2
    nsv5436735copy number variation1nstd206human GRCh38 chr1: 203,306,116-203,306,231 , GRCh37.p13 chr1: 203,275,244-203,275,359 BTG2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
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