btaf1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3901010	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 93,673,004-93,919,120 , GRCh38.p12 chr10: 91,913,247-92,159,363	BTAF1, SDHCP2, 3 more genes
nsv4456513	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 93,761,267-93,941,035 , GRCh38.p12 chr10: 92,001,510-92,181,278	BTAF1, CPEB3, 3 more genes
nsv4455624	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 93,707,316-93,925,053 , GRCh38.p12 chr10: 91,947,559-92,165,296	BTAF1, EIF4A1P8, 3 more genes
nsv4456865	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 93,723,462-93,941,035 , GRCh38.p12 chr10: 91,963,705-92,181,278	BTAF1, SDHCP2, 3 more genes
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	BTAF1, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	BTAF1, EIF2S2P3, 895 more genes
nsv3908115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627	BTAF1, EXOC6, 118 more genes
nsv6637868	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184	BTAF1, RPS27P1, 118 more genes
nsv7098887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213	BTAF1, LGI1, 79 more genes
nsv3901659	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,186,527-95,820,286 , GRCh38.p12 chr10: 91,426,770-94,060,529	BTAF1, NHP2P1, 48 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	BTAF1, 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	BTAF1, 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	BTAF1, 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	BTAF1, 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	BTAF1, EXOC6, 1906 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	BTAF1, LOC105378476, 688 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	BTAF1, SHOC2, 1487 more genes
nsv3894450	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537	BTAF1, HPS1, 422 more genes
nsv6637584	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 93,577,943-93,922,822 , GRCh38.p12 chr10: 91,818,186-92,163,065	BTAF1, EIF4A1P8, 5 more genes

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