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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6833549copy number variation1nstd229human GRCh38 chr7: 56,076,822-56,576,436 , GRCh37.p13 chr7: 56,144,515-56,644,129 NMD3P2, RNU6-1052P, 31 more genes
    nsv6824324copy number variation1nstd229human GRCh38 chr7: 56,447,811-56,624,522 , GRCh37.p13 chr7: 56,515,504-56,692,215 LOC100130210, RBM22P3, 12 more genes
    nsv6820603copy number variation1nstd229human GRCh38 chr7: 56,462,128-56,499,241 , GRCh37.p13 chr7: 56,529,821-56,566,934 RBM22P3, DKFZp434L192, 3 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
    nsv6632338copy number variation1nstd224human GRCh37 chr7: 56,509,323-56,689,209 , GRCh38.p12 chr7: 56,441,630-56,621,516 DKFZp434L192, LOC100419642, 12 more genes
    nsv6612988copy number variation1nstd223human GRCh38 chr7: 56,478,301-56,480,400 , GRCh37.p13 chr7: 56,545,994-56,548,093 LOC100240728
    nsv6612351copy number variation1nstd223human GRCh38 chr7: 56,334,501-56,612,800 , GRCh37.p13 chr7: 56,402,194-56,680,493 SEPTIN14P24, VN1R25P, 24 more genes
    nsv6605843copy number variation1nstd223human GRCh38 chr7: 56,447,811-56,624,522 , GRCh37.p13 chr7: 56,515,504-56,692,215 LOC101928401, LOC728376, 12 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6135773copy number variation1nstd213human GRCh37 chr7: 56,380,000-56,670,001 , GRCh38.p12 chr7: 56,312,307-56,602,308 LOC728376, LOC731631, 23 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5478344copy number variation1nstd206human GRCh38 chr7: 56,342,453-56,635,465 , GRCh37.p13 chr7: 56,410,146-56,703,158 DKFZp434L192, LOC650226, 24 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4704542copy number variation1nstd195human GRCh37 chr7: 56,469,301-56,556,751 , GRCh38.p12 chr7: 56,401,608-56,489,058 LOC650226, LOC728376, 4 more genes
    nsv4609065copy number variation1nstd183human GRCh37 chr7: 56,382,055-56,612,161 , GRCh38.p12 chr7: 56,314,362-56,544,468 VN1R24P, LOC100419642, 19 more genes
    nsv4455806copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,809,787-58,025,873 , GRCh38.p12 chr7: 52,742,093-57,966,167 RPL31P35, SEC61G, 161 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4401248copy number variation1nstd174human GRCh37 chr7: 56,453,095-56,835,595 , GRCh38.p12 chr7: 56,385,402-56,767,902 LOC100130210, RNU6-1052P, 22 more genes
    nsv4394401copy number variation1nstd174human GRCh37 chr7: 56,117,100-56,632,479 , GRCh38.p12 chr7: 56,049,407-56,564,786 IFITM3P4, VN1R25P, 34 more genes
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