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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143432copy number variation1nstd232human GRCh37.p13 chr1: 38,484,822-38,484,921 , GRCh38.p12 chr1: 38,019,150-38,019,249 UTP11
    nsv7142176insertion1nstd232human GRCh37.p13 chr1: 38,484,249-38,484,249 , GRCh38.p12 chr1: 38,018,577-38,018,577 UTP11
    nsv7140342insertion1nstd232human GRCh37.p13 chr1: 38,478,537-38,478,537 , GRCh38.p12 chr1: 38,012,865-38,012,865 UTP11
    nsv7138705insertion1nstd232human GRCh37.p13 chr1: 38,483,443-38,483,443 , GRCh38.p12 chr1: 38,017,771-38,017,771 UTP11
    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
    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
    nsv6649572copy number variation1nstd229human GRCh38 chr1: 37,745,813-38,046,235 , GRCh37.p13 chr1: 38,211,485-38,511,907 C1orf122, RPS2P13, 15 more genes
    nsv6649078copy number variation1nstd229human GRCh38 chr1: 37,894,301-38,107,800 , GRCh37.p13 chr1: 38,359,973-38,573,472 MIR3659, FHL3, 7 more genes
    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
    nsv4903371copy number variation1nstd200human GRCh38 chr1: 37,745,813-38,046,236 , GRCh37.p13 chr1: 38,211,485-38,511,908 FHL3, YRDC, 15 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4326932inversion1nstd166human GRCh37.p13 chr1: 35,173,490-93,458,530 , GRCh38.p12 chr1: 34,707,889-92,992,973 , ATP6V0B, 1069 more genes
    nsv3901163copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937 TMEM222, ZBTB8OS, 453 more genes
    nsv3886123copy number variation1nstd102humanLikely benign GRCh37 chr1: 37,766,562-38,727,114 , GRCh38.p12 chr1: 37,300,961-38,261,442 FHL3, DNALI1, 36 more genes
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