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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5864205copy number variation1nstd209human GRCh38 chr7: 114,994,089-114,999,161 , GRCh37.p13 chr7: 114,634,143-114,639,215 MDFIC
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5489419copy number variation1nstd206human GRCh38 chr7: 115,005,332-115,005,392 , GRCh37.p13 chr7: 114,645,386-114,645,446 MDFIC
    nsv5480675copy number variation1nstd206human GRCh38 chr7: 114,990,445-114,990,503 , GRCh37.p13 chr7: 114,630,499-114,630,557 MDFIC
    nsv5371034translocation1nstd200human GRCh38 chr7: 115,005,332-115,005,332 , GRCh38 chr7: 115,005,392-115,005,392 , GRCh37.p13 chr7: 114,645,446-114,645,446 , GRCh37.p13 chr7: 114,645,386-114,645,386 MDFIC
    nsv5371033translocation1nstd200human GRCh38 chr7: 114,990,503-114,990,503 , GRCh38 chr7: 114,990,445-114,990,445 , GRCh37.p13 chr7: 114,630,557-114,630,557 , GRCh37.p13 chr7: 114,630,499-114,630,499 MDFIC
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5249744copy number variation1nstd204human GRCh38.p13 chr7: 115,017,301-115,019,400 , GRCh37.p13 chr7: 114,657,355-114,659,454 MDFIC
    nsv5110388mobile element insertion1nstd203human GRCh38 chr7: 114,934,609-114,934,619 , GRCh37.p13 chr7: 114,574,664-114,574,674 MDFIC
    nsv5106065mobile element insertion1nstd203human GRCh38 chr7: 115,018,575-115,018,588 , GRCh37.p13 chr7: 114,658,629-114,658,642 MDFIC
    nsv5100273mobile element insertion1nstd203human GRCh38 chr7: 114,943,220-114,943,228 , GRCh37.p13 chr7: 114,583,275-114,583,283 MDFIC
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4965181copy number variation1nstd200human GRCh38 chr7: 114,926,162-114,973,486 , GRCh37.p13 chr7: 114,566,217-114,613,541 MDFIC
    nsv4951100copy number variation1nstd200human GRCh38 chr7: 114,994,413-115,011,501 , GRCh37.p13 chr7: 114,634,467-114,651,555 MDFIC
    nsv4951099copy number variation1nstd200human GRCh38 chr7: 114,959,242-114,962,557 , GRCh37.p13 chr7: 114,599,297-114,602,612 MDFIC
    nsv4951098copy number variation1nstd200human GRCh38 chr7: 114,929,258-114,933,323 , GRCh37.p13 chr7: 114,569,313-114,573,378 MDFIC
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825280copy number variation1nstd200human GRCh37 chr7: 114,566,217-114,613,541 , GRCh38.p12 chr7: 114,926,162-114,973,486 MDFIC
    nsv4820181copy number variation1nstd200human GRCh37 chr7: 114,569,313-114,573,378 , GRCh38.p12 chr7: 114,929,258-114,933,323 MDFIC
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