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Items: 1 to 20 of 608

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098709complex chromosomal rearrangement10nstd230human GRCh37 chr2: 138,497,728-138,497,728 , GRCh37 chr2: 138,497,728-138,497,728 , GRCh37 chr2: 229,140,446-229,140,446 , GRCh37 chr2: 229,140,448-229,140,448 , GRCh37 chr2: 230,000,005-230,000,005 , GRCh37 chr2: 230,000,008-230,000,008 , GRCh37 chr2: 230,813,287-230,813,287 , GRCh37 chr2: 230,813,290-230,813,290 , GRCh37 chr2: 232,570,621-232,570,621 , GRCh37 chr2: 232,570,621-232,570,621 , GRCh37 chr2: 232,578,683-232,578,683 , GRCh37 chr2: 232,578,683-232,578,683 , GRCh37 chr2: 233,231,729-233,231,729 , GRCh37 chr2: 233,231,871-233,231,871 , GRCh37 chr5: 155,645,550-155,645,550 , GRCh37 chr5: 165,720,606-165,720,606 , GRCh37 chr11: 76,745,560-76,745,560 , GRCh37 chr11: 76,745,561-76,745,561 , GRCh37 chr11: 95,030,214-95,030,214 , GRCh37 chr11: 95,030,221-95,030,221 , GRCh38.p12 chr11: 77,034,516-77,034,516 , GRCh38.p12 chr11: 77,034,517-77,034,517 , GRCh38.p12 chr11: 95,297,050-95,297,050 , GRCh38.p12 chr11: 95,297,057-95,297,057 , GRCh38.p12 chr2: 137,740,158-137,740,158 , GRCh38.p12 chr2: 137,740,158-137,740,158 , GRCh38.p12 chr2: 228,275,730-228,275,730 , GRCh38.p12 chr2: 228,275,732-228,275,732 , GRCh38.p12 chr2: 229,135,289-229,135,289 , GRCh38.p12 chr2: 229,135,292-229,135,292 , GRCh38.p12 chr2: 229,948,571-229,948,571 , GRCh38.p12 chr2: 229,948,574-229,948,574 , GRCh38.p12 chr2: 231,705,911-231,705,911 , GRCh38.p12 chr2: 231,705,911-231,705,911 , GRCh38.p12 chr2: 231,713,973-231,713,973 , GRCh38.p12 chr2: 231,713,973-231,713,973 , GRCh38.p12 chr2: 232,367,019-232,367,019 , GRCh38.p12 chr2: 232,367,161-232,367,161 , GRCh38.p12 chr5: 156,218,540-156,218,540 , GRCh38.p12 chr5: 166,293,601-166,293,601 PTMA, SGCD, 3 more genes
    nsv7055749inversion1nstd229human GRCh38 chr2: 229,978,765-229,980,330 , GRCh37.p13 chr2: 230,843,481-230,845,046 FBXO36
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv7050091inversion1nstd229human GRCh38 chr2: 229,892,462-229,996,054 , GRCh37.p13 chr2: 230,757,178-230,860,770 FBXO36, LOC105373924, 4 more genes
    nsv7049962inversion1nstd229human GRCh38 chr2: 227,539,172-230,370,061 , GRCh37.p13 chr2: 228,403,888-231,234,776 SPHKAP, TRIP12, 37 more genes
    nsv7046239inversion1nstd229human GRCh38 chr2: 229,826,292-229,956,702 , GRCh37.p13 chr2: 230,691,008-230,821,418 TRIP12, RNU6-964P, 3 more genes
    nsv7045442inversion1nstd229human GRCh38 chr2: 229,826,152-229,925,487 , GRCh37.p13 chr2: 230,690,868-230,790,203 RNU6-613P, TRIP12, 1 more genes
    nsv7043225inversion1nstd229human GRCh38 chr2: 229,996,055-230,082,490 , GRCh37.p13 chr2: 230,860,771-230,947,206 FBXO36, RNY4P19, 3 more genes
    nsv6697413copy number variation1nstd229human GRCh38 chr2: 229,927,168-230,201,826 , GRCh37.p13 chr2: 230,791,884-231,066,542 SP110, RNU6-964P, 8 more genes
    nsv6697104copy number variation1nstd229human GRCh38 chr2: 229,923,901-230,024,900 , GRCh37.p13 chr2: 230,788,617-230,889,616 LOC107985996, RNU6-964P, 3 more genes
    nsv6696858copy number variation1nstd229human GRCh38 chr2: 229,969,582-229,973,616 , GRCh37.p13 chr2: 230,834,298-230,838,332 RNU6-1027P, FBXO36
    nsv6696185copy number variation1nstd229human GRCh38 chr2: 230,011,901-230,015,000 , GRCh37.p13 chr2: 230,876,617-230,879,716 FBXO36
    nsv6694417copy number variation1nstd229human GRCh38 chr2: 229,931,901-229,954,573 , GRCh37.p13 chr2: 230,796,617-230,819,289 FBXO36, LOC105373924, 1 more genes
    nsv6693661copy number variation1nstd229human GRCh38 chr2: 229,963,701-229,972,200 , GRCh37.p13 chr2: 230,828,417-230,836,916 FBXO36, RNU6-1027P
    nsv6693222copy number variation1nstd229human GRCh38 chr2: 229,983,810-230,303,649 , GRCh37.p13 chr2: 230,848,526-231,168,364 SP110, RNY4P19, 5 more genes
    nsv6692923copy number variation1nstd229human GRCh38 chr2: 229,939,658-230,023,927 , GRCh37.p13 chr2: 230,804,374-230,888,643 LOC105373924, FBXO36, 2 more genes
    nsv6691617copy number variation1nstd229human GRCh38 chr2: 229,963,257-229,972,126 , GRCh37.p13 chr2: 230,827,973-230,836,842 FBXO36, RNU6-1027P
    nsv6691589copy number variation1nstd229human GRCh38 chr2: 229,933,885-229,937,352 , GRCh37.p13 chr2: 230,798,601-230,802,068 RNU6-964P, FBXO36
    nsv6690921copy number variation1nstd229human GRCh38 chr2: 229,888,601-230,011,100 , GRCh37.p13 chr2: 230,753,317-230,875,816 TRIP12, FBXO36, 4 more genes
    nsv6690424copy number variation1nstd229human GRCh38 chr2: 229,875,788-230,324,835 , GRCh37.p13 chr2: 230,740,504-231,189,550 RNU6-613P, SP110, 10 more genes
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