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Items: 1 to 20 of 27

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3911198copy number variation1nstd102humanUncertain significance GRCh37 chr4: 94,289,958-95,121,723 , GRCh38 chr4: 93,368,807-94,200,572 , NCBI36 chr4: 94,508,981-95,340,746 ATOH1, HMGB3P15, 3 more genes
    nsv3912037copy number variation2nstd102humanUncertain significance NCBI36 chr4: 93,653,365-95,211,397 , GRCh38 chr4: 92,513,191-94,071,223 , GRCh37 chr4: 93,434,342-94,992,374 ATOH1, RACK1P3, 3 more genes
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 ATOH1, EREG, 530 more genes
    nsv3923733copy number variation1nstd102humanPathogenic GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621 ATOH1, PDLIM5, 215 more genes
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 ATOH1, LOC105377327, 214 more genes
    nsv3888958copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500 ATOH1, LOC391674, 156 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 ATOH1, LOC105377329, 166 more genes
    nsv3912429copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,800,931-95,730,598 , NCBI36 chr4: 82,019,955-95,949,621 , GRCh38 chr4: 80,879,777-94,809,447 ATOH1, RNU6-469P, 152 more genes
    nsv3885328copy number variation1nstd102humanPathogenic GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651 ATOH1, TRMT10A, 86 more genes
    nsv3910689copy number variation1nstd102humanPathogenic GRCh38 chr4: 92,610,413-101,521,991 , GRCh37 chr4: 93,531,564-102,443,148 , NCBI36 chr4: 93,750,587-102,662,171 ATOH1, GRID2, 77 more genes
    nsv3910328copy number variation1nstd102humanPathogenic GRCh37 chr4: 86,370,518-94,894,345 , GRCh38 chr4: 85,449,365-93,973,194 , NCBI36 chr4: 86,589,542-95,113,368 ATOH1, LOC112268468, 81 more genes
    nsv3888291copy number variation1nstd102humanPathogenic GRCh37 chr4: 90,005,204-96,971,785 , GRCh38.p12 chr4: 89,084,053-96,050,634 ATOH1, HMGB3P15, 33 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 ATOH1, LOC100422029, 2358 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 ATOH1, LOC100420289, 2347 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 ATOH1, MTND4LP29, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 ATOH1, LOC112268460, 2345 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 ATOH1, LOC105377343, 2341 more genes
    nsv3875534copy number variation1nstd102humanPathogenic GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318 ATOH1, KLKB1, 1118 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 ATOH1, SNHG27, 1091 more genes
    nsv3913811copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792 ATOH1, LOC105377297, 582 more genes
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