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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098144copy number variation1nstd102humanUncertain significance GRCh37 chr7: 92,760,530-92,765,284 , GRCh38.p12 chr7: 93,131,217-93,135,971 SAMD9L
    nsv7097392copy number variation1nstd102humanUncertain significance GRCh37 chr7: 92,754,520-92,764,207 , GRCh38.p12 chr7: 93,125,207-93,134,894 SAMD9L
    nsv7055867inversion1nstd229human GRCh38 chr7: 93,142,637-93,150,345 , GRCh37.p13 chr7: 92,771,950-92,779,658 SAMD9L
    nsv7051078inversion1nstd229human GRCh38 chr7: 93,142,878-93,146,808 , GRCh37.p13 chr7: 92,772,191-92,776,121 SAMD9L
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv6830997copy number variation1nstd229human GRCh38 chr7: 93,140,107-93,140,397 , GRCh37.p13 chr7: 92,769,420-92,769,710 SAMD9L
    nsv6827433copy number variation1nstd229human GRCh38 chr7: 93,087,518-93,168,785 , GRCh37.p13 chr7: 92,716,831-92,798,098 SAMD9, SAMD9L
    nsv6826163copy number variation1nstd229human GRCh38 chr7: 92,216,103-93,815,120 , GRCh37.p13 chr7: 91,845,417-93,444,432 SAMD9, KRIT1, 23 more genes
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6313572copy number variation1nstd102humanUncertain significance GRCh37 chr7: 92,044,792-93,320,149 , GRCh38.p12 chr7: 92,415,478-93,690,837 CDK6-AS1, RNU6-10P, 20 more genes
    nsv6284055insertion1nstd214human GRCh38 chr7: 93,140,165-93,140,165 , GRCh37.p13 chr7: 92,769,478-92,769,478 SAMD9L
    nsv6142091copy number variation1nstd206human GRCh38 chr7: 93,146,758-93,150,392 , GRCh37.p13 chr7: 92,776,071-92,779,705 SAMD9L
    nsv6135795copy number variation1nstd213human GRCh37 chr7: 91,910,000-93,250,001 , GRCh38.p12 chr7: 92,280,686-93,620,689 ERVW-1, ANKIB1, 20 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv6062490insertion1nstd212human GRCh38 chr7: 93,140,116-93,140,116 , GRCh37.p13 chr7: 92,769,429-92,769,429 SAMD9L
    nsv5643633insertion1nstd207human GRCh38 chr7: 93,140,094-93,140,094 , GRCh37.p13 chr7: 92,769,407-92,769,407 SAMD9L
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