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Items: 1 to 20 of 185

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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
    nsv7095613copy number variation1nstd102humanUncertain significance GRCh37 chr1: 38,003,349-38,003,633 , GRCh38.p12 chr1: 37,537,748-37,538,032 SNIP1, LOC105378649
    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
    nsv6649564copy number variation1nstd229human GRCh38 chr1: 37,532,806-37,561,716 , GRCh37.p13 chr1: 37,998,407-38,027,317 SNIP1, DNALI1, 3 more genes
    nsv6649563copy number variation1nstd229human GRCh38 chr1: 37,509,005-37,559,946 , GRCh37.p13 chr1: 37,974,606-38,025,547 SNIP1, RPS27P9, 4 more genes
    nsv6649508copy number variation1nstd229human GRCh38 chr1: 37,546,157-37,551,017 , GRCh37.p13 chr1: 38,011,758-38,016,618 SNIP1
    nsv6649366copy number variation1nstd229human GRCh38 chr1: 37,548,186-37,548,279 , GRCh37.p13 chr1: 38,013,787-38,013,880 SNIP1
    nsv6649365copy number variation1nstd229human GRCh38 chr1: 37,538,013-37,540,158 , GRCh37.p13 chr1: 38,003,614-38,005,759 LOC105378649, SNIP1
    nsv6649364copy number variation1nstd229human GRCh38 chr1: 37,520,461-37,538,246 , GRCh37.p13 chr1: 37,986,062-38,003,847 LOC105378649, SNIP1
    nsv6332869copy number variation1nstd223human GRCh38 chr1: 37,532,319-37,535,245 , GRCh37.p13 chr1: 37,997,920-38,000,846 LOC105378649, SNIP1
    nsv6331866copy number variation1nstd223human GRCh38 chr1: 37,507,754-37,544,375 , GRCh37.p13 chr1: 37,973,355-38,009,976 SNIP1, LOC105378649, 2 more genes
    nsv6321340copy number variation1nstd223human GRCh38 chr1: 37,520,461-37,538,261 , GRCh37.p13 chr1: 37,986,062-38,003,862 SNIP1, LOC105378649
    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
    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
    nsv6059019insertion1nstd212human GRCh38 chr1: 37,536,149-37,536,149 , GRCh37.p13 chr1: 38,001,750-38,001,750 LOC105378649, SNIP1
    nsv6056963insertion1nstd212human GRCh38 chr1: 37,535,235-37,535,235 , GRCh37.p13 chr1: 38,000,836-38,000,836 LOC105378649, SNIP1
    nsv5965861insertion1nstd209human GRCh38 chr1: 37,535,230-37,535,230 , GRCh37.p13 chr1: 38,000,831-38,000,831 LOC105378649, SNIP1
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