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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6835809copy number variation1nstd229human GRCh38 chr7: 93,245,605-93,250,043 , GRCh37.p13 chr7: 92,874,918-92,879,356 VPS50
    nsv6834842copy number variation1nstd229human GRCh38 chr7: 93,228,482-93,231,085 , GRCh37.p13 chr7: 92,857,795-92,860,398 HEPACAM2, VPS50
    nsv6830016copy number variation1nstd229human GRCh38 chr7: 93,275,935-93,276,314 , GRCh37.p13 chr7: 92,905,247-92,905,626 VPS50
    nsv6829308copy number variation1nstd229human GRCh38 chr7: 93,317,701-93,323,000 , GRCh37.p13 chr7: 92,947,013-92,952,312 VPS50
    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
    nsv6825385copy number variation1nstd229human GRCh38 chr7: 93,218,141-93,578,061 , GRCh37.p13 chr7: 92,847,454-93,207,373 CALCR, MIR653, 4 more genes
    nsv6824201copy number variation1nstd229human GRCh38 chr7: 93,285,583-93,288,624 , GRCh37.p13 chr7: 92,914,895-92,917,936 VPS50
    nsv6821222copy number variation1nstd229human GRCh38 chr7: 93,354,073-93,357,941 , GRCh37.p13 chr7: 92,983,385-92,987,253 VPS50
    nsv6820756copy number variation1nstd229human GRCh38 chr7: 93,263,873-93,264,224 , GRCh37.p13 chr7: 92,893,185-92,893,536 VPS50
    nsv6820611copy number variation1nstd229human GRCh38 chr7: 93,276,086-93,276,412 , GRCh37.p13 chr7: 92,905,398-92,905,724 VPS50
    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
    nsv6632407copy number variation1nstd224human GRCh37 chr7: 92,809,993-93,347,267 , GRCh38.p12 chr7: 93,180,680-93,717,955 CALCR, VPS50, 6 more genes
    nsv6620045copy number variation1nstd223human GRCh38 chr7: 93,247,534-93,247,924 , GRCh37.p13 chr7: 92,876,847-92,877,237 VPS50
    nsv6619405copy number variation1nstd223human GRCh38 chr7: 93,243,701-93,244,600 , GRCh37.p13 chr7: 92,873,014-92,873,913 VPS50
    nsv6618702copy number variation1nstd223human GRCh38 chr7: 93,288,615-93,289,196 , GRCh37.p13 chr7: 92,917,927-92,918,508 VPS50
    nsv6618239copy number variation1nstd223human GRCh38 chr7: 93,354,995-93,355,687 , GRCh37.p13 chr7: 92,984,307-92,984,999 VPS50
    nsv6617255copy number variation1nstd223human GRCh38 chr7: 93,312,633-93,316,019 , GRCh37.p13 chr7: 92,941,945-92,945,331 VPS50
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