slc16a9[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	SLC16A9, RNU7-12P, 1876 more genes
nsv4675455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325	SLC16A9, MRLN, 242 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	SLC16A9, UNC5B-AS1, 250 more genes
nsv4675436	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 56,031,210-65,660,398 , GRCh38.p12 chr10: 54,271,450-63,900,638	SLC16A9, MRPL35P2, 77 more genes
nsv4675795	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 55,589,950-63,990,649 , GRCh38.p12 chr10: 53,830,190-62,230,890	SLC16A9, ARL4AP1, 52 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	SLC16A9, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	SLC16A9, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	SLC16A9, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	SLC16A9, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	SLC16A9, EXOC6, 1906 more genes
nsv3924859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961	SLC16A9, BMS1P4-AGAP5, 471 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	SLC16A9, SLC9A3P3, 476 more genes
nsv3921181	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433	SLC16A9, AGAP6, 338 more genes
nsv3919727	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 55,287,177-67,558,442 , GRCh37 chr10: 57,046,937-69,318,200 , NCBI36 chr10: 56,716,943-68,988,206	SLC16A9, RNU6-543P, 96 more genes
nsv3905569	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 57,587,928-64,212,007 , GRCh38.p12 chr10: 55,828,168-62,452,248	SLC16A9, ANK3, 48 more genes
nsv3923539	inversion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279	SLC16A9, ALOX5, 248 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	SLC16A9, SHOC2, 1487 more genes
nsv6637363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 57,941,252-64,846,332 , GRCh38.p12 chr10: 56,181,491-63,086,572	SLC16A9, TMEM26-AS1, 53 more genes
nsv6637322	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 60,870,153-63,790,451 , GRCh38.p12 chr10: 59,110,393-62,030,692	SLC16A9, MRPL50P4, 25 more genes
nsv4455623	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 59,199,424-62,981,900 , GRCh38.p12 chr10: 57,439,664-61,222,142	SLC16A9, FAM133CP, 35 more genes

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Items: 20

Number of Variants: 20

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