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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7095992copy number variation1nstd102humanUncertain significance GRCh37 chr1: 38,003,349-38,273,852 , GRCh38.p12 chr1: 37,537,748-37,808,180 LOC105378650, ACTN4P2, 15 more genes
    nsv7054252inversion1nstd229human GRCh38 chr1: 37,623,969-37,625,924 , GRCh37.p13 chr1: 38,089,641-38,091,596 RSPO1
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649568copy number variation1nstd229human GRCh38 chr1: 37,621,801-37,640,600 , GRCh37.p13 chr1: 38,087,473-38,106,272 RSPO1
    nsv6649512copy number variation1nstd229human GRCh38 chr1: 37,628,832-37,631,926 , GRCh37.p13 chr1: 38,094,504-38,097,598 RSPO1
    nsv6649511copy number variation1nstd229human GRCh38 chr1: 37,621,262-37,624,816 , GRCh37.p13 chr1: 38,086,934-38,090,488 RSPO1
    nsv6649510copy number variation1nstd229human GRCh38 chr1: 37,617,415-37,620,270 , GRCh37.p13 chr1: 38,083,087-38,085,942 RSPO1
    nsv6328210copy number variation1nstd223human GRCh38 chr1: 37,628,829-37,631,923 , GRCh37.p13 chr1: 38,094,501-38,097,595 RSPO1
    nsv6327416copy number variation1nstd223human GRCh38 chr1: 37,617,436-37,620,250 , GRCh37.p13 chr1: 38,083,108-38,085,922 RSPO1
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6212211insertion1nstd214human GRCh38 chr1: 37,611,748-37,611,748 , GRCh37.p13 chr1: 38,077,349-38,077,349 RSPO1
    nsv6133994copy number variation1nstd213human GRCh37 chr1: 37,480,000-43,930,001 , GRCh38.p12 chr1: 37,014,399-43,464,330 BMP8B, CDC20, 183 more genes
    nsv6052653insertion1nstd212human GRCh38 chr1: 37,629,486-37,629,486 , GRCh37.p13 chr1: 38,095,158-38,095,158 RSPO1
    nsv6045531insertion1nstd212human GRCh38 chr1: 37,611,748-37,611,748 , GRCh37.p13 chr1: 38,077,349-38,077,349 RSPO1
    nsv5952934insertion1nstd209human GRCh38 chr1: 37,611,748-37,611,748 , GRCh37.p13 chr1: 38,077,349-38,077,349 RSPO1
    nsv5609770insertion1nstd207human GRCh38 chr1: 37,611,748-37,611,748 , GRCh37.p13 chr1: 38,077,349-38,077,349 RSPO1
    nsv5553785insertion1nstd206human GRCh38 chr1: 37,611,748-37,611,799 , GRCh37.p13 chr1: 38,077,349-38,077,471 RSPO1
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