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Items: 1 to 20 of 430

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5330276translocation1nstd200human GRCh37 chr7: 76,072,449-76,072,449 , GRCh37 chr7: 76,209,495-76,209,495 , GRCh38.p12 chr7: 76,580,178-76,580,178 , GRCh38.p12 chr7|NT_187561.1: 67,013-67,013 , GRCh38.p12 chr7: 76,443,132-76,443,132 LINC03009
    nsv4825082copy number variation1nstd200human GRCh37 chr7: 76,330,117-76,332,641 , GRCh38.p12 chr7|NT_187561.1: 187,635-190,159 , GRCh38.p12 chr7: 76,700,800-76,703,324
    nsv4811978copy number variation1nstd200human GRCh37 chr7: 76,251,029-76,253,595 , GRCh38.p12 chr7: 76,621,712-76,624,278 , GRCh38.p12 chr7|NT_187561.1: 108,547-111,113 POMZP3, LINC03009
    nsv4746065copy number variation1nstd199human GRCh37 chr7: 76,245,883-76,246,185 , GRCh38.p12 chr7: 76,616,566-76,616,868 , GRCh38.p12 chr7|NT_187561.1: 103,401-103,703 LINC03009, POMZP3
    nsv4742020copy number variation1nstd199human GRCh37 chr7: 76,209,674-76,209,731 , GRCh38.p12 chr7: 76,580,357-76,580,414 , GRCh38.p12 chr7|NT_187561.1: 67,192-67,249 LINC03009
    nsv4737809copy number variation1nstd199human GRCh37 chr7: 76,336,275-76,336,327 , GRCh38.p12 chr7: 76,706,958-76,707,010 , GRCh38.p12 chr7|NT_187561.1: 193,793-193,845
    nsv4728030copy number variation1nstd197human GRCh37 chr7: 76,240,783-76,241,130 , GRCh38.p12 chr7: 76,611,466-76,611,813 , GRCh38.p12 chr7|NT_187561.1: 98,301-98,648 POMZP3, LINC03009
    nsv4723056insertion1nstd186human GRCh37 chr7: 76,291,828-76,291,828 , GRCh38.p12 chr7: 76,662,511-76,662,511 , GRCh38.p12 chr7|NT_187561.1: 149,346-149,346
    nsv4690823mobile element insertion1nstd186human GRCh37 chr7: 76,291,838-76,291,838 , GRCh38.p12 chr7: 76,662,521-76,662,521 , GRCh38.p12 chr7|NT_187561.1: 149,356-149,356
    nsv4679108copy number variation1nstd189human GRCh37.p13 chr7: 76,123,485-76,521,617 , GRCh38.p12 chr7: 76,494,168-76,892,300 , GRCh38.p12 chr7|NT_187561.1: 1-209,586 , POMZP3, 7 more genes
    nsv4669307copy number variation1nstd186human GRCh37 chr7: 76,173,056-76,224,552 , GRCh38.p12 chr7: 76,543,739-76,595,235 , GRCh38.p12 chr7|NT_187561.1: 30,576-82,070 SPDYE1, LINC03009
    nsv4659364copy number variation1nstd186human GRCh37 chr7: 76,173,056-76,224,552 , GRCh38.p12 chr7: 76,543,739-76,595,235 , GRCh38.p12 chr7|NT_187561.1: 30,576-82,070 LINC03009, SPDYE1
    nsv4657042copy number variation1nstd186human GRCh37 chr7: 76,260,000-76,265,000 , GRCh38.p12 chr7: 76,630,683-76,635,683 , GRCh38.p12 chr7|NT_187561.1: 117,518-122,518 0
    nsv4656799copy number variation3nstd186human GRCh37 chr7: 76,677,000-76,684,000 , GRCh38.p12 chr7: 77,047,683-77,054,683 , GRCh38.p12 chr7|NT_187561.1: 15,498-22,512 SPDYE1, PMS2P9, 1 more genes
    nsv4656578copy number variation1nstd186human GRCh37 chr7: 76,313,000-76,323,000 , GRCh38.p12 chr7: 76,683,683-76,693,683 , GRCh38.p12 chr7|NT_187561.1: 170,518-180,518
    nsv4652734copy number variation1nstd186human GRCh37 chr7: 76,260,734-76,263,752 , GRCh38.p12 chr7: 76,631,417-76,634,435 , GRCh38.p12 chr7|NT_187561.1: 118,252-121,270 0
    nsv4651901copy number variation1nstd186human GRCh37 chr7: 76,676,200-76,682,200 , GRCh38.p12 chr7: 77,046,883-77,052,883 , GRCh38.p12 chr7|NT_187561.1: 14,698-20,699 SPDYE1, PMS2P9, 2 more genes
    nsv4651694copy number variation1nstd186human GRCh37 chr7: 76,171,000-76,236,250 , GRCh38.p12 chr7: 76,541,683-76,606,933 , GRCh38.p12 chr7|NT_187561.1: 28,844-93,768 LINC03009, SPDYE1
    nsv4650968copy number variation1nstd186human GRCh37 chr7: 76,185,149-76,197,165 , GRCh38.p12 chr7|NT_187561.1: 42,667-54,683 , GRCh38.p12 chr7: 76,555,832-76,567,848 LINC03009
    nsv4649687copy number variation1nstd186human GRCh37 chr7: 76,175,200-76,180,300 , GRCh38.p12 chr7: 76,545,883-76,550,983 , GRCh38.p12 chr7|NT_187561.1: 32,716-37,817 SPDYE1, LINC03009
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