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Items: 1 to 20 of 836

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137714copy number variation1nstd232human GRCh37.p13 chr2: 229,949,574-229,949,658 , GRCh38.p12 chr2: 229,084,858-229,084,942 PID1
    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
    nsv7056201inversion1nstd229human GRCh38 chr2: 229,246,871-229,248,775 , GRCh37.p13 chr2: 230,111,587-230,113,491 PID1
    nsv7050230inversion1nstd229human GRCh38 chr2: 229,030,098-229,033,390 , GRCh37.p13 chr2: 229,894,814-229,898,106 PID1
    nsv7049962inversion1nstd229human GRCh38 chr2: 227,539,172-230,370,061 , GRCh37.p13 chr2: 228,403,888-231,234,776 SPHKAP, TRIP12, 37 more genes
    nsv6698063copy number variation1nstd229human GRCh38 chr2: 229,242,162-229,251,063 , GRCh37.p13 chr2: 230,106,878-230,115,779 PID1
    nsv6697669copy number variation1nstd229human GRCh38 chr2: 229,092,053-229,092,238 , GRCh37.p13 chr2: 229,956,769-229,956,954 PID1
    nsv6695751copy number variation1nstd229human GRCh38 chr2: 228,915,440-229,390,482 , GRCh37.p13 chr2: 229,780,156-230,255,198 PID1, RN7SKP283, 2 more genes
    nsv6695195copy number variation1nstd229human GRCh38 chr2: 229,093,038-229,093,509 , GRCh37.p13 chr2: 229,957,754-229,958,225 PID1
    nsv6695130copy number variation1nstd229human GRCh38 chr2: 229,084,847-229,084,943 , GRCh37.p13 chr2: 229,949,563-229,949,659 PID1
    nsv6694245copy number variation1nstd229human GRCh38 chr2: 229,020,853-229,023,456 , GRCh37.p13 chr2: 229,885,569-229,888,172 PID1
    nsv6694183copy number variation1nstd229human GRCh38 chr2: 229,085,319-229,094,658 , GRCh37.p13 chr2: 229,950,035-229,959,374 PID1
    nsv6694152copy number variation1nstd229human GRCh38 chr2: 229,192,437-229,203,625 , GRCh37.p13 chr2: 230,057,153-230,068,341 PID1
    nsv6693212copy number variation1nstd229human GRCh38 chr2: 229,153,248-229,153,490 , GRCh37.p13 chr2: 230,017,964-230,018,206 PID1
    nsv6693105copy number variation1nstd229human GRCh38 chr2: 229,163,668-229,163,697 , GRCh37.p13 chr2: 230,028,384-230,028,413 PID1
    nsv6693100copy number variation1nstd229human GRCh38 chr2: 229,043,434-229,046,075 , GRCh37.p13 chr2: 229,908,150-229,910,791 PID1
    nsv6690167copy number variation1nstd229human GRCh38 chr2: 229,259,310-229,263,720 , GRCh37.p13 chr2: 230,124,026-230,128,436 PID1
    nsv6689471copy number variation1nstd229human GRCh38 chr2: 229,141,686-229,142,418 , GRCh37.p13 chr2: 230,006,402-230,007,134 PID1
    nsv6689416copy number variation1nstd229human GRCh38 chr2: 229,249,190-229,249,312 , GRCh37.p13 chr2: 230,113,906-230,114,028 PID1
    nsv6687686copy number variation1nstd229human GRCh38 chr2: 229,069,533-229,069,939 , GRCh37.p13 chr2: 229,934,249-229,934,655 PID1
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